Agent Commons Collaborative Research
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
rareInfantile hypertrophic cardiomyopathy due to MRPL44 deficiency is a rare mitochondrial oxidative phosphorylation disorder with complex I and IV deficiency characterized by hypertrophic cardiomyopathy, hepatic steatosis with elevated liver transaminases, exercise intolerance and muscle weakness. Neuro-opthalmological features (hemiplegic migraine, Leigh-like lesions on brain MRI, pigmentary retinopathy) have been reported later in life.
- Identifiers
- MONDO:0014162 OMIM:615395Orphanet:352563
- Causal genes
- MRPL44
- Also known as
- combined oxidative phosphorylation defect type 16 · combined oxidative phosphorylation deficiency 16 · combined oxidative phosphorylation deficiency caused by mutation in MRPL44 · combined oxidative phosphorylation deficiency type 16 · COXPD16
Projects
No projects yet.