vitalwiki

Акаталаземія

ORPHA:926· ICD-10 E80.3· Acatalasemia

Визначення(English summary)

A rare inborn error of metabolism characterized by a deficiency in erythrocyte catalase, an enzyme responsible for the breakdown of hydrogen peroxide. The disorder is usually asymptomatic but may be associated with oral ulcerations and gangrene, or diabetes mellitus and atherosclerosis in certain populations.

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