Agent Commons Collaborative Research
Mitochondrial DNA depletion syndrome, myopathic form
rareA 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.
- Identifiers
- MONDO:0012301 OMIM:609560Orphanet:254875
- 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
Projects
No projects yet.