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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease congenital fiber type disproportion
Comorbidity C0270960|congenital myopathy
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PubMedID- 21267004 In this study, we report a 30-year longitudinal clinical survey of a patient harboring a novel severe and complex phenotype, combining an early-onset progeroid syndrome and a congenital myopathy with fiber-type disproportion.

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