Clinical Trial Update: Natural History in CCFDN and IBM Syndromes

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Summary

This completed observational study from Ludwig-Maximilians-University Munich examines the natural history of Congenital cataracts, facial dysmorphism, and neuro…

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Diseases / indications

• Autosomal-dominant Inclusion Body Myopathy
• Autosomal-recessive Inclusion Body Myopathy
• Congenital Cataracts Facial Dysmorphism and Neuropathy
• Inclusion Body Myositis

Snippet

Sponsor: Ludwig-Maximilians - University of Munich | Conditions: Inclusion Body Myositis, Sporadic, Inclusion Body Myopathy, Autosomal-recessive | Status: COMPLETED