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Alpha Thalassemia in Children What is alpha thalassemia in children? Alpha thalassemia is an inherited blood disorder. This means it is passed down through the parent’s genes. It may cause anemia in their children. Anemia is low numbers of red blood cells or low hemoglobin level

Beta Thalassemia in Children What is beta thalassemia in children? Beta thalassemia is an inherited blood disorder. This means it's passed down through a parent’s genes. It's a form of anemia. Anemia is a low red blood cell or low hemoglobin level. Hemoglobin is part of red blood

Thalassemia Click on the links below to learn more about this topic. Alpha Thalassemia Beta Thalassemia (Cooley's Anemia)© 2000-2025 The StayWell Company, LLC. All rights reserved. This information is not intended as a substitute for professional medical care. Always follow your

Sepsis in the Newborn What is newborn sepsis? Newborn sepsis is a severe infection in an infant younger than 28 days old. The infection is in your baby’s blood. But it may affect any body system or the whole body. What causes newborn sepsis? Newborn sepsis is most often caused by

Congenital Heart Disease According to the American Heart Association, about 9 of every 1,000 babies born in the U.S. have a congenital heart defect. This is a problem that occurs as the baby's heart is developing during pregnancy, before the baby is born. Congenital heart defects

Failure to Thrive (FTT) in Children What is failure to thrive in children? Failure to thrive (FTT) is slow physical development in a baby or child. It’s caused by a baby or child not having enough nutrition. FTT is a clinical observation, not a diagnosis. It is used to describe a

Ventricular Septal Defect (VSD) What is a ventricular septal defect? A ventricular septal defect (VSD) is a congenital heart defect. This means that your baby is born with it. A VSD is a hole in the wall (septum) that separates the 2 lower chambers of the heart (right and left

Overview of Craniofacial Anomalies What are craniofacial anomalies? Craniofacial anomalies (CFA) are a variety of deformities in the growth of the head and facial bones. Anomaly is a medical term meaning different from normal. These abnormalities are present at birth (congenital)

The Craniofacial Team When should my child see a craniofacial team? The best time for the first assessment of craniofacial abnormalities is within your child's first few weeks of life. The focus of the team visit is to help correct your child's medical problems and to ease

Hemifacial Microsomia (HFM) in Children What is hemifacial microsomia in children? Hemifacial microsomia (HFM) is a congenital problem. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped. (Hemi means half). HFM usually