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Learning Center
Congenital heart defects in children
Learn about symptoms, tests and treatments for children born with a problem in the structure of the heart.
Choroid plexus carcinoma
This rare type of cancerous brain tumor occurs mainly in children under 2. Treatment usually involves surgery and radiation therapy.
Ehlers-Danlos syndrome
Learn about these complex genetic disorders that cause problems with connective tissue in the skin, joints and blood vessel walls.
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.
Epilepsy
Learn about this condition that causes seizures. Find out which symptoms are associated with different types of seizures and how they're treated.
Pyloric stenosis
In this condition, a valve between an infant's stomach and small intestine fails to open enough for food to pass through. Surgery is the treatment.
Klinefelter syndrome
This genetic disorder occurs when a male is born with an extra copy of the X chromosome and may result in low testosterone production and infertility.
Ureteral obstruction
Learn about what causes blockage of the tubes that carry urine from the kidneys to the bladder, tests you might need and how the condition can be treated.
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.
Spina bifida
Learn about this condition in which an unborn baby's spine and spinal cord don't form properly. Surgery during pregnancy may be a treatment option.
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