Infant health
Learning Center
Ebstein anomaly
In this rare heart defect, the tricuspid heart valve didn't form properly. This can affect the heart's ability to pump blood. Know the risks and symptoms.
Metachromatic leukodystrophy
This rare genetic disorder causes fatty substances (sulfatides) to build up in your brain and nervous system, causing progressive loss of nerve function.
Congenital adrenal hyperplasia
This group of inherited genetic conditions limits the adrenal glands' ability to make certain vital hormones.
Epidermolysis bullosa
Learn about a rare inherited disease that often shows up in infancy and causes fragile, blistering skin on the palms and feet. Severe disease may be fatal.
Shaken baby syndrome
Understand why shaking a baby can cause brain damage, and why getting immediate medical care can save a child’s life or prevent serious health problems.
Ambiguous genitalia
Learn about causes and treatment of ambiguous genitalia, a rare disorder of sex development in which a baby's external genitals are not clearly male or female.
Arteriovenous malformation
In this condition, a tangle of blood vessels affects the flow of blood and oxygen. Treatment can help.
Neuroblastoma
Learn more about the symptoms, diagnosis and treatment of neuroblastoma, one of the most common cancers of childhood.
Congenital heart defects in children
Learn about symptoms, tests and treatments for children born with a problem in the structure of the heart (congenital heart defect).
Hydronephrosis
Learn about this condition that occurs when urine doesn't drain properly from the upper urinary tract, leading to kidney swelling.
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