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Хвороба Хартнупа

ORPHA:2116· ICD-10 E72.0· Hartnup disease

Визначення(English summary)

A rare metabolic disorder belonging to the neutral aminoacidurias, mainly characterized by skin photosensitivity, ocular and neuropsychiatric features, due to abnormal renal and gastrointestinal transport of neutral amino acids (tryptophan, alanine, asparagine, glutamine, histidine, isoleucine, leucine, phenylalanine, serine, threonine, tyrosine and valine).

Поширеність
1-9 / 100 000
Успадкування
Autosomal recessive
Вік початку
All ages