An Overview Of Anencephaly
Feb 06, 2024 | 12 comments Reference
What Is Anencephaly And How Prevalent Is It Among Infants?
Anencephaly is a rare birth defect that affects the development of the brain and skull of a fetus. It occurs in approximately 1 out of every 10,000 pregnancies and is one of the most common neural tube defects. Anencephalic babies are born with an underdeveloped brain and often have parts of their skull missing. It is a serious condition that is usually fatal within hours or days after birth. Despite this, it has been estimated that up to 8% of all stillborn infants may have had anencephaly at some point during their development. This article will discuss what anencephaly is, its prevalence among infants, as well as possible causes and treatments for this condition. Anencephaly is characterized by the underdeveloped brain of a fetus.
Anencephaly results in children being born with an undeveloped cerebellum, which is located on the bottom front portion of your brain. This cerebellum is responsible for many functions such as equilibrium and muscle coordination. Without it, children with anencephaly often have difficulty moving and are also unable to manage basic reflexes such as blinking or swallowing due to their lack of balance or coordination.
Navigating Bowel Atresias In Infancy & Pregnancy
jan 15, 2024 | 18 comments Reference
What Are Bowel Atresias And How Common Are They?
Bowel atresia is a congenital condition in which the small intestine does not form correctly, leading to an obstruction in the intestines. It is one of the most common gastrointestinal birth defects, affecting 1 in 6,000 live births. There are several types of bowel atresia, including jejunal atresia, ileal atresia, and gastroschisis. These conditions can cause serious medical problems and require immediate treatment.
What is bowel atresia? A bowel atresia is a condition in which the small intestine does not form correctly, leading to an obstruction in the intestines. It can lead to other complications like malabsorption and infection, which could cause significant health problems and even death. There are several types of bowel atresia including jejunal atresia, ileal atresia, and gastroschisis.
There are several potential symptoms of bowel atresia including fever, lochia (blood loss), vomiting, diarrhea, weight loss, and abdominal pain. Bowel atresia may be diagnosed before birth through a combination of ultrasound and fetal echocardiogram. In other cases, the diagnosis is made after birth through abdominal or chest x-ray.
Congenital Pulmonary Airway Malformation (CPAM)
jan 15, 2024 | 10 comments Reference
How do they affect the brain?
Congenital Pulmonary Airway Malformation (CPAM) is a fetal lung malformation that occurs during the development of the lungs in utero. It is a rare condition, but can be life-threatening if not identified and treated early. CPAM affects the structure of the lungs, causing them to be underdeveloped or malformed, resulting in airway blockage and difficulty breathing. In this article, we will discuss what CPAM is and how it develops in order to better understand this condition.
How Does CPAM Develop? Pulmonary Airway Malformations typically develop during fetal development, around nine weeks after conception. These problems may occur when certain cells in the embryo are damaged due to oxygen deprivation during a particular stage of gestation: before, during or after the thirteen-week mark. The cells that are damaged may become disrupted and then further develop into cystic tissue, which obstructs the airway or passage of fluid (lung)The other type of CPAM is a congenital obstruction of the peripheral bronchial tree. This is due to a defect in either later stages of embryo development or as a result of chromosome abnormalities in early prenatal development.
Common Causes & Symptoms of CPAM Congenital Pulmonary Airway Malformation (CPAM) is a condition that affects the lungs of newborns and is characterized by the presence of cysts or sacs in the lung tissue. It often results in respiratory distress, collapsed lung, and meconium aspiration syndrome. CPAM can be caused by genetic mutations, environmental factors, or a combination of both. How do they typically present? A common presentation of this condition is with a loud snoring or stridor that occurs during sleep, typically in infants and young children. The most common symptoms of CPAM are those related to the heart and lungs: Tachypnea (rapid breathing) and other signs suggesting
Cardiac disease that causes difficulty breathing usually affects the lungs first. If a heart defect prevents blood from reaching the lungs and blood vessels in the brainstem and cerebellum, oxygen levels in those areas of the brain can be decreased. In turn, this can result in sleepiness during childhood as well as attention-deficit/hyperactivity disorder (ADHD).
Diagnostic Tests for CPAM Congenital Pulmonary Airway Malformation (CPAM) is a rare lung disorder that can be diagnosed with the help of imaging tests. These tests include antenatal ultrasound scanning, chest x-ray and Magnetic Resonance Imaging (MRI). Each of these tests has its own advantages and disadvantages in diagnosing CPAM. The antenatal ultrasound scan is used to detect the presence of CPAM during pregnancy, while chest x-rays and MRI scans are used to assess the extent of the malformation after birth. Depending on the test results, further treatment may be recommended for CPAM patients.
Discordant Growth In Pregnancy
jan 15, 2024 | 10 comments Reference
What Is Discordant Growth In Pregnancy And Why Is It Important For Us To Know
Discordant growth in pregnancy is a condition where the fetus does not grow at the same rate as it should during pregnancy. This can be due to either Intrauterine Growth Restriction (IUGR) or Fetal Macrosomia (FGM). IUGR is a condition where the fetus is smaller than normal for its gestational age, while FGM occurs when the fetus is larger than normal for its gestational age. Both of these conditions can have serious implications for both mother and baby, making it important to identify discordant growth in pregnancy. Ultrasound scans are routinely used to monitor fetal growth, and any changes in fetal size should be investigated further.
Aneuploidy Screening In Pregnancy
Dec 30, 2023 | 10 comments Reference
What Is Aneuploidy And How Does It Affect Prenatal Health.?
What Is Aneuploidy? Aneuploidy is a genetic abnormality that affects the number of chromosomes in a cell, resulting in an abnormal chromatin structure. It is one of the most common causes of birth defects and can have a significant impact on prenatal health. This article will explore what aneuploidy is and how it can affect prenatal health. We will discuss the different types of aneuploidy, its diagnosis, and potential treatments or management strategies. Finally, we will look at how aneuploidy can be prevented to ensure healthy pregnancies for mothers and babies. Aneuploidy is a genetic abnormality that affects the chromosome number in a cell. It occurs when there is an abnormal number of chromosomes in the nucleus, which can lead to various health problems during pregnancy. This genetic abnormality can affect the chromatin structure of cells and cause them to be unable to function properly. As a result, it can have serious consequences for prenatal health, including birth defects and developmental delays. In this article, we will discuss how aneuploidy affects prenatal health and what measures can be taken to prevent it from occurring.
Serious Consequences Of Delayed Diagnosis During Pregnancy
Dec 30, 2023 | 10 comments Reference
Delayed diagnosis during pregnancy is a situation where a pregnant woman does not receive timely medical care or treatment for her condition. This can be dangerous for both the mother and the unborn baby as it can lead to serious health complications. Prenatal screening tests are important in helping to diagnose any potential issues early on, which is why prenatal care is so important. Late diagnosis during pregnancy can cause serious medical issues, such as birth defects, developmental delays, and even death in some cases. It is essential that pregnant women get regular prenatal care and follow-up screenings to ensure their health and the health of their unborn baby. . Delayed diagnosis usually follows a pattern of not receiving care or treatment for an ailment, such as problems with pregnancy. Symptoms might include pain, bleeding, or other problems that could lead to serious health complications/issues. It is important during prenatal care to make sure any potential issues are caught and addressed early on so they can be treated before they become more severe. Early diagnosis is beneficial for both the mother and the unborn baby as it could lead to a more favorable outcome. Symptoms tend to be less severe, which can reduce the risk of developing a potentially life-threatening condition. Regular prenatal care also provides education, guidance, and support for mothers through their pregnancy. Prenatal care helps build healthy relationships with both mother and baby that can last after childbirth. It is important during pregnancy to make sure any potential problems are caught early on in order to prevent complications from arising later on in the pregnancy (such as those mentioned below) or even after birth in some cases.
Dec 28, 2023 | 10 comments Reference
Prenatal diagnosis is a medical process that involves testing for any potential health issues in a fetus before it is born. It is important because it can detect any genetic or physical abnormalities in the fetus and allow parents to make informed decisions about the pregnancy. Prenatal diagnosis also helps doctors to provide timely care and treatment if needed. The most common types of antenatal testing include amniocentesis, chorionic villus sampling (CVS), ultrasound, and blood tests. These tests can help identify any potential risks or complications in the pregnancy, such as chromosomal abnormalities, birth defects, and genetic disorders. Knowing these risks ahead of time allows parents to make informed decisions about their pregnancy and ensure that they are providing their baby with the best possible care.
Amniocentesis is a test that requires more samples of amniotic fluid surrounding the fetus in order to test for chromosomal abnormalities. It can detect Down syndrome or other chromosomal conditions, such as trisomy 18 or trisomy 13. The procedure involves taking a needle and extracting amniotic fluid near the baby's head, which is then sent to the lab for testing. If there are chromosomal abnormalities, doctors may recommend terminating the pregnancy and giving birth to a child with special needs.
Mid-Trimester Targeted Scans In Pregnancy
Dec 25, 2023 | 10 comments Reference
Mid-trimester targeted scans are an important part of pregnancy care. A Mid-trimester Targeted Scan is an ultrasound scan that is usually done between weeks 18 and 22 of pregnancy. It is a detailed scan of the fetus and its surrounding structures, giving us a better insight into the anatomy and development of the baby. The scan helps to identify any potential risks or abnormalities in the fetus, as well as to assess growth and development. These ultrasound scans help to assess the health of both the mother and the fetus, as well as providing valuable information for making decisions about care during pregnancy. The benefits of mid-trimester targeted scans include providing information about fetal growth and development, detecting any potential birth defects or other health issues, and helping to monitor the mother’s health. Furthermore, these scans can help to identify any risks that may be present during pregnancy or labor. By having a better understanding of the mother’s and baby’s health, mid-trimester targeted scans can ensure that both are provided with optimal care throughout the pregnancy period. The mid-trimester scan can be used to diagnose any conditions that would require intervention during labor and delivery. For example, it can reveal a condition such as spina bifida or anencephaly, which would make having a natural birth difficult and requires the baby to be delivered via cesarean section. It is also used for the purpose of screening for genetic conditions so that parents can decide whether the risk of having more children is worth it.
A Comprehensive Guide To Fetal Viability Scans In India: Best Practices & Cost Estimation
Dec 05, 2023 | 6 comments Reference
What Is A Fetal Viability Scan And When Should It Be Conducted?
What is a viability scan? A viability scan is a medical test that can be used to assess the health of the developing fetus in utero. It involves using ultrasound to determine if there are any signs that the baby may need emergency, or non-urgent, intervention. If an abnormality is found, it can cause an increase in fetal distress and it will be necessary for a more invasive procedure to be performed on the baby. Can I do an early fetal viability scan at home? Yes, you can purchase a home pregnancy test kit and perform your own early fetal viability scans at home. These kits generally have a window where you can do a scan..