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