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Inherited metabolic disorders
Caused by gene changes, these disorders affect the body's ability to change food into energy. They also affect how energy is used, such as for cell repair.
Klippel-Trenaunay syndrome
Main signs of this congenital disorder involve a red birthmark (port-wine stain), vein malformations, and overgrowth of tissues and bones.
Neuroblastoma
Learn more about the symptoms, diagnosis and treatment of neuroblastoma, one of the most common cancers of childhood.
Patent ductus arteriosus (PDA)
Learn about symptoms, causes and treatment of this common — and treatable — heart problem that occurs shortly after birth.
Phenylketonuria (PKU)
PKU is caused by a change in the gene that helps create an enzyme needed to break down phenylalanine. Treatment includes a special diet and medication.
Pulmonary atresia
This life-threatening heart condition that's present at birth changes the way blood travels from the heart to the rest of the body.
Reye's syndrome
Learn about the causes and treatment of this rare but serious condition causing swelling in the liver and brain.
Tongue-tie (ankyloglossia)
With tongue-tie (ankyloglossia), a band of tissue (frenulum) tethers the tongue, restricting the range of motion. Learn about symptoms and treatment.
Tricuspid atresia
Learn how this congenital heart defect blocks blood flow from the heart to the lungs. Treatment involves multiple surgeries.
Turner syndrome
Turner syndrome affects only females as the result of a missing or partially missing X chromosome, causing a variety of medical and developmental problems.
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