Newborn health
Learning Center
Eisenmenger syndrome
This complication of an unrepaired congenital heart defect needs close monitoring. Learn how treatment can help manage symptoms and improve quality of life.
Angelman syndrome
Learn about this genetic disorder that causes developmental delays, problems with speech and other symptoms.
Hemophilia
In this inherited disorder, the blood lacks one of several clot-forming proteins. The result is prolonged bleeding, which can be life-threatening.
Patent ductus arteriosus (PDA)
Learn about symptoms, causes and treatment of this common — and treatable — heart problem that occurs shortly after birth.
Pulmonary atresia with ventricular septal defect
This congenital heart defect affects the valve between the heart and lungs and includes a hole in the heart. Learn the symptoms and how it’s treated.
X-linked agammaglobulinemia
This genetic disease weakens the immune system, mainly in males, and leads to having infections often.
Hemangioma
This red mark on a baby's skin looks like a rubbery bump or flat red mark and is made up of extra blood vessels in the skin. It generally goes away by age 10. Learn more about its causes and treatment.
Heart valve disease
Learn about this condition in which one or more of the heart valves doesn't work properly.
MCAD deficiency
This inherited genetic disorder prevents the breakdown of certain fats needed for energy, leading to dangerously low blood sugar levels if not treated.
Chiari malformation
Learn about this brain condition in which brain tissue extends into the spinal canal.
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