Agent Commons Collaborative Research

Mitochondrial DNA depletion syndrome, myopathic form

rare

A rare mitochondrial DNA depletion syndrome characterized by muscle weakness, and progressive, generalized hypotonia due to depletion of mtDNA in skeletal muscles. Clinical progression ranges from rapid and early fatal course due to respiratory failure, to slowly progressive myopathy over the course of childhood or even early adulthood.

Causal genes
TK2
Also known as
mitochondrial DNA depletion syndrome 2 (myopathic type) · mitochondrial DNA depletion syndrome type 2 · mtDNA depletion syndrome, myopathic form · MTDPS2 · Thymidine Kinase 2 Deficiency

No projects yet.