Medical services

Our dedicated team of sonographers and healthcare professionals are committed to providing unparalleled maternal-fetal ultrasound services, ensuring the highest standard of care for expecting families.

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A woman getting prenatal care and an ultrasound for fetal diagnostics to monitor high risk pregnancy

Ultrasound

Imaging procedures that utilize sound waves to create real-time images of the fetus, enabling us to monitor fetal development, detect any abnormalities, and provide expectant parents with visual updates on their baby's progress during pregnancy.

Nuchal Translucency Ultrasound

Nuchal translucency ultrasound is a specialized prenatal screening test performed during the first trimester of pregnancy, typically between weeks 12 and 14.  This ultrasound evaluates the thickness of the nuchal fold, a clear space at the back of the fetus's neck. An increased nuchal translucency measurement may indicate a higher risk of certain chromosomal abnormalities, such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), or Patau syndrome (trisomy 13). While an increased nuchal translucency measurement does not provide a definitive diagnosis, it may prompt further diagnostic testing, such as chorionic villus sampling (CVS) or amniocentesis, to confirm or rule out the presence of a chromosomal abnormality. Nuchal translucency ultrasound is a safe and non-invasive screening tool that provides valuable information to expectant parents about their baby's health and allows for informed decision-making regarding prenatal care.

First, second, and third trimester anatomical survey

The first, second, and third-trimester anatomical surveys are comprehensive ultrasound examinations performed during specific stages of pregnancy to assess the growth and development of the fetus and to detect any potential structural abnormalities. The first-trimester anatomical survey, often conducted around 12-14 weeks of gestation, focuses on evaluating fetal anatomy, measuring nuchal translucency, and assessing the risk of chromosomal abnormalities. The second-trimester anatomical survey, typically performed between 18 and 22 weeks, involves a detailed examination of fetal anatomy, including the brain, spine, heart, limbs, and abdominal organs, to identify any potential congenital anomalies. Additionally, this scan evaluates the placenta, amniotic fluid levels, and the cervix. The third-trimester anatomical survey, usually conducted around 28-32 weeks, assesses fetal growth, amniotic fluid volume, and placental function, while also checking for any late-developing structural abnormalities. These anatomical surveys play a crucial role in monitoring fetal health and development throughout pregnancy, enabling our team of healthcare providers to provide appropriate management and counseling to expectant parents.

Advanced 3D/4D Ultrasound

Advanced 3D/4D ultrasound technology represents an innovative approach to prenatal imaging, providing detailed, three-dimensional (3D) visualizations of the developing fetus in real-time. Unlike traditional 2D ultrasounds, which produce flat, two-dimensional images, advanced 3D/4D ultrasound allows for the creation of high-resolution, lifelike images and videos that offer a more comprehensive view of the baby's anatomy and movements. This technology utilizes sound waves to generate detailed images of the fetus, allowing healthcare providers to assess fetal growth and development, detect any structural abnormalities, and provide expectant parents with a deeper understanding and connection to their unborn child. Additionally, 4D ultrasound provides the added dimension of time, capturing dynamic movements such as fetal facial expressions, hand gestures, and body movements in real-time. While advanced 3D/4D ultrasound is primarily used for prenatal imaging and bonding purposes, it can also aid in diagnosing certain fetal abnormalities and guiding medical interventions when necessary. Overall, advanced 3D/4D ultrasound offers a unique and valuable tool for enhancing the prenatal experience and promoting maternal-fetal bonding.

Fetal Echocardiography

Fetal echocardiography is a specialized ultrasound examination performed during pregnancy to evaluate the structure and function of the fetal heart. This advanced imaging technique provides detailed, real-time images of the fetal heart, allowing healthcare providers to assess cardiac anatomy, detect any structural abnormalities, and evaluate heart function and blood flow patterns. Fetal echocardiography is typically recommended when there is an increased risk of congenital heart defects due to factors such as family history of heart disease, maternal diabetes, or abnormal findings on routine prenatal ultrasound. By identifying cardiac abnormalities early in pregnancy, fetal echocardiography enables our team of healthcare providers to provide expectant parents with accurate diagnoses, counseling, and appropriate management plans, including referral to specialized pediatric cardiology centers for further evaluation and intervention if necessary. Overall, fetal echocardiography plays a crucial role in prenatal care, allowing for timely detection and management of congenital heart defects and promoting the best possible outcomes for affected infants.

Multiple Gestation Imaging

Multiple gestation imaging refers to the specialized ultrasound examinations performed during pregnancy to assess the development and well-being of multiple fetuses, such as twins, triplets, or higher-order multiples. These ultrasound scans are tailored to address the unique challenges and complexities associated with multiple pregnancies, including monitoring fetal growth, assessing placental function, and identifying any potential complications such as twin-to-twin transfusion syndrome (TTTS) or twin reversed arterial perfusion (TRAP sequence). Multiple gestation imaging plays a crucial role in prenatal care, allowing our team of healthcare providers to monitor the health and development of each fetus individually, detect any structural abnormalities or growth discrepancies, and provide appropriate management and counseling to expectant parents. Close monitoring and specialized care are essential to optimize outcomes for both the mother and the babies in multiple pregnancies, and multiple gestation imaging serves as a valuable tool in achieving this goal.

Doppler Studies

Doppler studies in pregnancy refer to a specialized type of ultrasound examination used to assess blood flow within the maternal and fetal circulatory systems. By utilizing Doppler ultrasound technology, these studies measure the speed and direction of blood flow in various vessels, providing valuable insights into the vascular health of both the mother and the developing fetus. Doppler studies are commonly employed to evaluate blood flow in the umbilical artery, uterine artery, and fetal middle cerebral artery, among others. These assessments help our team of healthcare providers to detect abnormalities such as placental insufficiency, fetal distress, or intrauterine growth restriction, which can impact pregnancy outcomes. By identifying such issues early, Doppler studies enable healthcare teams to implement appropriate interventions and closely monitor pregnancies to optimize the health and well-being of both the mother and the baby.

High-Risk Pregnancy

A high-risk pregnancy refers to a pregnancy where there are potential complications that could pose risks to the health of the mother, the baby, or both, requiring specialized medical care and monitoring.

Pregnancy Complications

Pregnancy complications encompass a broad spectrum of health issues that can arise during gestation, impacting the well-being of both the mother and the developing fetus. These complications vary in severity and may include conditions such as gestational diabetes, preeclampsia, placenta previa, preterm labor, miscarriage, and fetal growth restriction. Factors such as maternal age, pre-existing health conditions, lifestyle choices, genetic predispositions, and environmental factors can contribute to their development. Early detection, proper medical management, and timely intervention are crucial in mitigating risks and ensuring optimal outcomes for both mother and baby. We believe that close monitoring by our dedicated healthcare professionals, strict adherence to prenatal care guidelines, and open communication between you, the expectant mother, and our healthcare team are crucial elements in effectively managing and addressing any pregnancy complications that may arise. Your health and the well-being of your baby are our top priorities, and we are committed to providing you with the highest quality care every step of the way.

Genetic Counseling

Genetic counseling in high-risk pregnancies is an essential service that helps expectant parents understand the potential genetic conditions or abnormalities that could affect their baby. It involves a thorough evaluation of the family's medical history, genetic screening, and diagnostic tests to identify potential risks. Genetic counselors provide guidance on the implications of test results, helping parents make informed decisions about their pregnancy. For those with a history of genetic disorders, advanced maternal age, or other risk factors, genetic counseling offers valuable insights and support, ensuring the best possible care throughout the pregnancy.

Cancer and pregnancy

If you currently have cancer, had cancer previously, or you’re at an increased risk of developing cancer during pregnancy, this affects your prenatal care. We discuss how to balance all aspects of your pregnancy and cancer diagnosis or risk to optimize your and your baby’s health. Our experienced team is well-equipped to help you navigate the complexities of managing both your cancer treatment and the health of your pregnancy. Through close monitoring, adherence to prenatal care guidelines, and open communication, we will work together to develop a personalized care plan that prioritizes both your well-being and the health of your baby. Your strength and resilience inspire us, and we are committed to providing you with the highest quality of care to ensure the best possible outcomes for you and your growing family.

Cardiovascular disease and pregnancy

Cardiovascular disease during pregnancy refers to any pre-existing or newly developed heart conditions that affect expectant mothers. These conditions may include but are not limited to, hypertension, congenital heart defects, valvular heart disease, arrhythmias, and cardiomyopathies. Pregnancy imposes significant physiological changes on the cardiovascular system, placing additional stress on the heart. As a result, women with pre-existing heart conditions may experience exacerbation of symptoms or complications during pregnancy. Proper management and close monitoring are essential to ensure the health and safety of both the mother and the developing fetus. Our team will work closely with pregnant individuals to develop personalized care plans, which may include medication management, lifestyle modifications, and specialized prenatal care, to optimize outcomes and minimize risks associated with cardiovascular disease during pregnancy. Early detection, timely intervention, and ongoing communication between the patient and our healthcare team are crucial for a successful pregnancy outcome.

Diabetes and other endocrine disorders

Diabetes and other endocrine disorders in pregnancy encompass a range of conditions related to the endocrine system, such as diabetes mellitus, thyroid disorders, and adrenal gland disorders, that can affect pregnant individuals. Diabetes, including both type 1 and type 2 diabetes, presents unique challenges during pregnancy due to fluctuations in blood sugar levels and increased risk of complications for both the mother and baby. Similarly, thyroid disorders, such as hyperthyroidism or hypothyroidism, can impact maternal health and fetal development if not properly managed. Our team are experts in caring for women with diabetes and other endocrine disorders. Early detection, proactive management, and ongoing communication between you and our healthcare providers are critical components in navigating diabetes and other endocrine disorders in pregnancy.

Fetal abnormalities

Fetal abnormalities refer to structural or functional anomalies present in a developing fetus during pregnancy. These abnormalities can affect various organs, systems, or body parts, and may arise due to genetic factors, environmental exposures, or unknown causes. Common fetal abnormalities include congenital heart defects, neural tube defects, chromosomal abnormalities (such as Down syndrome), skeletal deformities, and abnormalities of the gastrointestinal or urinary systems. While some fetal abnormalities are minor and may not significantly impact the baby's health or development, others can pose serious risks and may require medical intervention or specialized care. We offer prenatal screening and diagnostic tests, such as ultrasound scans, amniocentesis, and genetic testing, which play a crucial role in detecting fetal abnormalities early in pregnancy, allowing us to offer appropriate counseling, monitoring, and interventions to optimize outcomes for both the baby and the expectant mother. Early detection and comprehensive prenatal care are essential in managing fetal abnormalities and supporting families through the pregnancy journey.

Genetic disorders

Genetic disorders in pregnancy encompass a broad spectrum of conditions caused by abnormalities in the genes, sometimes inherited from one or both parents. These disorders can range from chromosomal abnormalities, such as Down syndrome, to single gene disorders like cystic fibrosis or sickle cell anemia. Genetic disorders can have varying degrees of impact on the health and development of the fetus, ranging from mild to severe. We offer prenatal screening and diagnostic tests, including genetic counseling, carrier screening, and advanced genetic testing, which play a crucial role in identifying genetic disorders early in pregnancy. With early detection, we offer expectant parents personalized counseling and options for further testing, intervention, and management strategies. While genetic disorders can present challenges during pregnancy, advancements in medical technology and genetic research have enabled our healthcare team to provide comprehensive care and support to families facing these conditions, ultimately striving to optimize outcomes for both the baby and the expectant mother.

Infections in pregnancy

Diabetes and other endocrine disorders in pregnancy encompass a range of conditions related to the endocrine system, such as diabetes mellitus, thyroid disorders, and adrenal gland disorders, that can affect pregnant individuals. Diabetes, including both type 1 and type 2 diabetes, presents unique challenges during pregnancy due to fluctuations in blood sugar levels and increased risk of complications for both the mother and baby. Similarly, thyroid disorders, such as hyperthyroidism or hypothyroidism, can impact maternal health and fetal development if not properly managed. Our team are experts in caring for women with diabetes and other endocrine disorders. Early detection, proactive management, and ongoing communication between you and our healthcare providers are critical components in navigating diabetes and other endocrine disorders in pregnancy.

Multifetal pregnancies

Multifetal pregnancies, also known as multiple pregnancies or pregnancies with more than one fetus, occur when a woman carries two or more babies simultaneously. These pregnancies can result from the release and fertilization of multiple eggs during ovulation (dizygotic or fraternal twins) or from the division of a single fertilized egg into two or more embryos (monozygotic or identical twins). Multifetal pregnancies can also involve triplets, quadruplets, or higher-order multiples. While multifetal pregnancies bring joy and excitement, they also present unique challenges and increased risks for both the mother and the babies. Complications associated with multifetal pregnancies include preterm birth, low birth weight, twin to twin transfusion syndrome, gestational diabetes, preeclampsia, placental abnormalities, and congenital anomalies. Our healthcare team ensures proper prenatal care, including close monitoring and specialized medical attention, which is essential to optimize outcomes for both the mother and the babies in multifetal pregnancies. We work closely with expectant parents to address any concerns, manage potential risks, and provide support throughout the pregnancy journey.

Placental problems

Placental problems encompass a range of conditions affecting the placenta, the vital organ that nourishes and supports the developing fetus during pregnancy. These problems can include placenta previa, where the placenta partially or completely covers the cervix, placental abruption, where the placenta detaches from the uterine wall prematurely, and placenta accreta, where the placenta attaches too deeply into the uterine wall. Placental problems can lead to complications such as vaginal bleeding, preterm birth, fetal growth restriction, and maternal hemorrhage. Our healthcare team focuses on timely detection and management of placental problems, which are crucial to minimizing risks and optimizing outcomes for both the mother and the baby. Close monitoring during prenatal care, along with appropriate medical interventions when necessary, play a key role in addressing placental problems and ensuring a healthy pregnancy.

Hypertension

Hypertension in pregnancy refers to high blood pressure that develops during gestation and can have significant implications for both the mother and the baby. This condition can manifest as either chronic hypertension, present before pregnancy or diagnosed before 20 weeks of gestation, or gestational hypertension, which arises after 20 weeks of pregnancy in previously normotensive women. Additionally, preeclampsia, a serious complication characterized by high blood pressure and signs of damage to other organ systems, can develop in women with or without pre-existing hypertension. Hypertension in pregnancy increases the risk of complications such as preterm birth, intrauterine growth restriction, placental abruption, and eclampsia, which can have severe consequences for both maternal and fetal health. Our healthcare team ensures close monitoring, timely intervention, and management of blood pressure levels are essential to mitigate risks and ensure the best possible outcomes for mother and baby.

Preeclampsia/Toxemia

Preeclampsia, also known as toxemia, is a serious pregnancy complication characterized by high blood pressure and signs of damage to other organ systems, typically occurring after 20 weeks of gestation. This condition can manifest as proteinuria (protein in the urine), kidney dysfunction, liver abnormalities, and blood clotting problems. Preeclampsia can progress to eclampsia, a life-threatening condition marked by seizures, which poses significant risks to both the mother and the baby. While the exact cause of preeclampsia is not fully understood, it is believed to involve abnormalities in the placenta, immune system, and blood vessels. Risk factors for preeclampsia include a history of the condition, first-time pregnancy, maternal age over 35, obesity, and certain medical conditions like diabetes and hypertension. Early detection through regular prenatal care and monitoring of blood pressure and urine protein levels is crucial in managing preeclampsia and preventing complications. Treatment may involve close monitoring, medications to lower blood pressure, and timely delivery of the baby in severe cases. Our healthcare team are experts in effectively managing preeclampsia and ensuring the health and safety of both mother and baby.

Cholestasis of Pregnancy

Cholestasis of pregnancy is a liver disorder characterized by decreased or blocked bile flow during pregnancy, leading to a buildup of bile acids in the bloodstream. This condition typically occurs in the second or third trimester and is associated with symptoms such as intense itching, particularly on the hands and feet. Cholestasis of pregnancy can increase the risk of complications for both the mother and the baby, including preterm birth, fetal distress, and stillbirth. While the exact cause is not fully understood, hormonal changes during pregnancy are thought to play a role in disrupting bile flow. Our healthcare team ensures close monitoring and management of cholestasis of pregnancy, which are essential to reduce the risk of complications. Treatment may involve medications to alleviate itching, monitoring fetal well-being through non-stress tests and ultrasound, and potentially early delivery if complications arise.

Preterm Birth

Preterm birth refers to the delivery of a baby before 37 weeks of gestation, instead of the typical 40-week duration of a full-term pregnancy. This occurrence can be spontaneous, resulting from factors such as premature labor or preterm rupture of membranes, or medically indicated due to maternal or fetal health concerns. Preterm birth poses significant risks to the health and development of the baby, as premature infants may have immature organ systems and are more vulnerable to complications such as respiratory distress syndrome, feeding difficulties, jaundice, and neurological issues. Additionally, preterm birth can also increase the risk of long-term health problems and developmental delays. We closely monitor pregnancies to identify and manage risk factors associated with preterm birth, such as multiple gestations, maternal health conditions like hypertension or diabetes, infections, and lifestyle factors like smoking or substance abuse. Early detection, timely intervention, and specialized neonatal care are essential in improving outcomes for preterm infants and reducing the potential for long-term complications.

Cerclage Placement

Cerclage placement is a surgical procedure performed during pregnancy to reinforce the cervix and prevent it from opening prematurely. This procedure is typically recommended for women who have a history of cervical insufficiency or have experienced previous preterm births due to cervical weakness. During cerclage placement, a stitch or band is placed around the cervix to provide mechanical support and help maintain its integrity throughout the remainder of the pregnancy. Cerclage placement is usually performed between weeks 12 and 24 of gestation, depending on individual circumstances. The goal of cerclage placement is to reduce the risk of cervical dilation and premature delivery, thus improving the chances of carrying the pregnancy to term and reducing the potential for complications associated with preterm birth. Our team of healthcare providers will work closely with you during this time, which is essential after cerclage placement to ensure the cervix remains stable and the pregnancy progresses safely.

Cephalic Version

Cephalic version is a medical procedure performed during pregnancy to manually reposition a breech or transverse fetus into a head-down, or cephalic, position within the uterus. Typically attempted during the late third trimester, cephalic version is often recommended for women whose babies remain in a breech or transverse presentation close to term. During the procedure, our team of healthcare providers use gentle pressure on the mother's abdomen to encourage the fetus to rotate into the desired position. Cephalic version is typically conducted under ultrasound guidance to ensure the safety of both the mother and the baby. By facilitating the optimal positioning of the fetus before labor begins, cephalic version can increase the likelihood of a vaginal delivery and reduce the need for a cesarean section, which may be necessary if the baby remains in a breech or transverse position. Close monitoring before, during, and after the procedure is essential to assess fetal well-being and ensure the success of the version attempt.

Growth Problems

Growth problems in pregnancy refer to conditions where the fetus does not develop at the expected rate or does not reach the anticipated size for its gestational age. These issues can manifest as either fetal growth restriction (FGR), where the fetus fails to achieve its genetic growth potential, or macrosomia, where the fetus grows larger than expected. FGR may result from various factors such as placental insufficiency, maternal health conditions like hypertension or diabetes, infections, smoking, or nutritional deficiencies. Conversely, macrosomia is often associated with maternal diabetes, excessive maternal weight gain, or genetic factors. Both FGR and macrosomia can pose risks during pregnancy and childbirth, including an increased likelihood of complications such as preterm birth, cesarean delivery, or neonatal complications. Early detection through regular prenatal monitoring, including ultrasound scans to assess fetal growth, is essential in identifying growth problems and implementing appropriate management strategies to optimize outcomes for both the mother and the baby.

Allo-immunization

Allo-immunization in pregnancy occurs when a pregnant woman's immune system produces antibodies that target antigens on the red blood cells of her fetus. This typically happens when there is a mismatch between the blood types of the mother and baby, such as when the mother is Rh-negative and the baby is Rh-positive. Allo-immunization can also occur in other blood group systems, such as the Kell, Duffy, or Kidd systems. When these antibodies cross the placenta, they can lead to hemolytic disease of the fetus and newborn (HDFN), a condition characterized by the destruction of the fetus's red blood cells, which can cause anemia, jaundice, and other complications. To prevent HDFN, Rh-negative women are often given Rh immunoglobulin (RhIg) during pregnancy and after delivery to prevent the development of Rh antibodies. Our team of healthcare providers offer close monitoring and specialized care that are essential for pregnant women at risk of allo-immunization to minimize the risk of complications for both the mother and the baby.

Non-stress Testing

Non-stress testing (NST) is a prenatal monitoring technique used to assess the well-being of the fetus during pregnancy. Typically performed in the third trimester, NST involves the use of external monitors to track fetal heart rate patterns and uterine contractions over a period of time, usually 20-30 minutes. During the test, fetal heart rate accelerations in response to fetal movement are considered reassuring, indicating that the baby's central nervous system is functioning properly and receiving adequate oxygenation. NST is often recommended for pregnant women with high-risk factors, such as gestational diabetes, hypertension, or decreased fetal movement, to evaluate fetal health and detect any signs of distress. A non-reactive NST, where fetal heart rate accelerations are not observed, may prompt further evaluation or additional testing to ensure the well-being of the fetus. Non-stress testing is a safe and non-invasive procedure that plays a valuable role in prenatal care, helping our team of healthcare providers monitor fetal health and make informed decisions to optimize outcomes for both mother and baby.

Diagnostic Screenings

Utilize advanced imaging technologies to provide detailed visual assessments of the fetus's growth, development, and overall health.

Cervical Length Screening

Cervical length screening is a crucial diagnostic procedure used to assess the length and integrity of the cervix during pregnancy. Typically performed via transvaginal ultrasound, this screening helps to evaluate the risk of preterm birth by measuring the cervical canal’s length and detecting any signs of cervical shortening or incompetence. A normal cervical length generally suggests a lower risk of preterm labor, while a shortened cervix may indicate a higher risk and necessitate further monitoring or intervention. By identifying potential issues early, cervical length screening enables healthcare providers to implement timely interventions, such as progesterone treatment or a cervical cerclage, to help reduce the risk of premature delivery and promote a healthier pregnancy outcome.

Genetic Screening

Genetic screening in pregnancy allows our team to offer personalized counseling, early detection, and informed decision-making to expectant parents, ultimately empowering them to make choices that best meet their individual needs and preferences. Genetic screening in pregnancy involves a range of tests used to assess the risk of certain genetic conditions or chromosomal abnormalities in the developing fetus. These tests are typically offered to pregnant individuals, especially those with risk factors such as advanced maternal age, family history of genetic disorders, or abnormal prenatal screening results.

Carrier Screening

Carrier screening in pregnancy is a type of genetic testing offered to individuals or couples planning to have children to assess their risk of passing on certain genetic disorders to their offspring. This screening is typically performed before conception or early in pregnancy and involves analyzing the DNA of the prospective parents to determine if they carry genetic mutations associated with inherited conditions such as cystic fibrosis, sickle cell disease, Tay-Sachs disease, and thalassemia, among others. Carrier screening helps identify individuals who are carriers of these genetic mutations, meaning they have one copy of the mutated gene but do not typically show symptoms of the associated disorder. However, if both prospective parents are carriers of the same genetic mutation, there is a risk that their child may inherit two copies of the mutated gene, resulting in the development of the genetic disorder. Carrier screening allows individuals or couples to make informed decisions about family planning, including the option of pursuing further testing or interventions to mitigate the risk of passing on genetic disorders to their children.

Cell-free DNA screening (noninvasive prenatal testing or NIPT)

Cell-free DNA screening, also known as noninvasive prenatal testing (NIPT), is a cutting-edge genetic screening method used during pregnancy to assess the risk of certain chromosomal abnormalities in the developing fetus. This noninvasive test analyzes fragments of fetal DNA circulating in the mother's bloodstream, which are derived from the placenta. By analyzing these cell-free DNA fragments, NIPT can detect the presence of extra or missing chromosomes, such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome), with a high degree of accuracy. NIPT can also provide information about the baby's sex and assess the risk of certain genetic conditions caused by specific chromosomal deletions or duplications. As a highly accurate and low-risk screening option, NIPT is often offered to pregnant individuals, especially those with advanced maternal age or other risk factors for chromosomal abnormalities. While NIPT is a powerful tool for prenatal screening, it is important to note that it is not a diagnostic test and may require confirmation through invasive diagnostic procedures such as amniocentesis or chorionic villus sampling (CVS) if abnormal results are detected. Overall, NIPT provides expectant parents with valuable information about their baby's health and allows them to make informed decisions about their pregnancy care.

Diagnostic Procedures

A range of medical tests and screenings conducted to assess the health and development of the fetus, identify any potential complications or abnormalities, and provide expectant parents with valuable information to guide their pregnancy journey.

Amniocentesis

Amniocentesis is a medical procedure performed during pregnancy to obtain a sample of amniotic fluid from the uterus for diagnostic purposes. Typically conducted between weeks 15 and 20 of gestation, amniocentesis involves the insertion of a thin needle through the mother's abdomen and into the amniotic sac under ultrasound guidance. The collected amniotic fluid contains fetal cells, which can be analyzed to detect chromosomal abnormalities, genetic disorders, neural tube defects, and other fetal anomalies. Amniocentesis is often recommended for women with certain risk factors, such as advanced maternal age, abnormal prenatal screening results, or a family history of genetic conditions. While amniocentesis carries a small risk of complications, such as infection or leakage of amniotic fluid, the procedure provides valuable information that can help expectant parents make informed decisions about their pregnancy, including options for prenatal care, management, and planning for the baby's future health needs.

Chorionic Villus Sampling (CVS)

Chorionic villus sampling (CVS) is a prenatal diagnostic procedure used to obtain a small sample of placental tissue from the chorionic villi, which are tiny finger-like projections on the placenta. Typically performed between weeks 10 and 13 of pregnancy, CVS involves the insertion of a thin needle or catheter either through the mother's abdomen or cervix, guided by ultrasound imaging, to access the chorionic villi. The collected tissue sample contains genetic material from the developing fetus, which can be analyzed to detect chromosomal abnormalities, genetic disorders, and other fetal anomalies. CVS is often recommended for women with certain risk factors, such as advanced maternal age, abnormal prenatal screening results, or a family history of genetic conditions. While CVS carries a small risk of complications, such as miscarriage or infection, the procedure provides valuable diagnostic information that can help expectant parents make informed decisions about their pregnancy, including options for prenatal care, management, and planning for the baby's future health needs.

Pre-pregnancy

Pre-pregnancy planning involves optimizing health and lifestyle choices to ensure the best outcomes for both mother and baby during conception and pregnancy.

Pre-pregnancy Consultations

Pre-pregnancy consultations are an essential step for individuals or couples planning to conceive, providing an opportunity to optimize health before conception. During these consultations, we will review medical histories, assess existing health conditions, and offer personalized advice on diet, lifestyle, and any necessary vaccinations or screenings. This proactive approach helps identify and address potential risks or complications, ensuring that both partners are in the best possible health to support a successful pregnancy. Additionally, these consultations can offer guidance on prenatal vitamins, fertility awareness, and family planning, setting the stage for a healthier pregnancy journey and better outcomes for both the parent and the baby.

Gestational Surrogacy Clearance Consultations

Gestational surrogacy clearance consultations are crucial steps in the process of engaging a surrogate to carry a pregnancy for intended parents. These consultations involve thorough medical and psychological evaluations to ensure the surrogate is physically and emotionally prepared for the role. Medical clearance includes comprehensive health screenings to confirm that the surrogate is in good health and capable of handling the demands of pregnancy, while psychological evaluations assess mental and emotional readiness. Additionally, legal and ethical aspects are reviewed to ensure that all parties understand and agree to the terms of the surrogacy arrangement. These consultations help to mitigate risks and establish a supportive framework, ensuring that the surrogacy process is safe, ethical, and successful for everyone involved.