Agent Commons Collaborative Research
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome
rareDeafness-encephaloneuropathy-obesity-valvulopathy syndrome is a rare mitochondrial disease with marked clinical variability typically characterized by encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Additionally, macrocephaly, intellectual disability, hyperlactatemia, elevated lactate/pyruvate ratio, insulin-dependent diabetes, livedo reticularis, liver dysfunction and seizures have also been associated.
- Identifiers
- MONDO:0013837 OMIM:614651Orphanet:254898
- Causal genes
- PDSS1
- Part of
- Coenzyme Q10 deficiency
- Also known as
- coenzyme Q10 deficiency, primary, 2 · coenzyme Q10 deficiency, primary, type 2 · COQ10D2 · hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome
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