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Синдром виснаження мітохондріальної ДНК, енцефаломіопатична форма

ORPHA:254803· Mitochondrial DNA depletion syndrome, encephalomyopathic form

Визначення(English summary)

Mitochondrial DNA depletion syndrome, encephalomyopathic form is a group of mitochondrial DNA maintenance syndrome diseases characterized by predominantly neuromuscular manifestations with typically infantile onset of hypotonia, lactic acidosis, psychomotor delay, progressive hyperkinetic-dystonic movement disorders, external ophtalmoplegia, sensosineural hearing loss, generalized seizures and variable renal tubular dysfunction. It may be associated with a broad range of other clinical features.

Успадкування
Autosomal recessive
Вік початку
Infancy, Neonatal