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Гіпертриптофанемія

ORPHA:2224· ICD-10 E70.8· Hypertryptophanemia

Визначення(English summary)

A rare inborn error of metabolism characterized by congenital hypertryptophanemia and hyperserotonemia. Patients are typically asymptomatic, although developmental delay, intellectual disability, and behavioral abnormalities, among others, have been reported in association.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Childhood, Infancy, Neonatal