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Інфантильна гіпертрофічна кардіоміопатія, зумовлена дефіцитом MRPL44

ORPHA:352563· ICD-10 E88.8· Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency

Визначення(English summary)

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.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Infancy, Neonatal