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PedAM

Pediatric Disease Annotations & Medicines




Disease myopathy
Phenotype C0268238|chanarin-dorfman syndrome
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PubMedID- 20676808 Among the disorders of lipid metabolism, mutations in the genes encoding two triglyceride lipases acting hand in hand cause severe generalized lipid storage myopathy, one associated with ichthyosis (chanarin-dorfman syndrome), the other dominated by juvenile-onset weakness.

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