Natural History in CCFDN and IBM Syndromes

Inclusion Body Myositis, Sporadic Clinical Trial

Official title: Retrospective Cohort Study Assessing the Natural Course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and Sporadic and Hereditary Inclusion Body Myopathies (IBM)

Status Completed

Clinical Trial Summary

So far, only limited data is available regarding the natural course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and sporadic and hereditary inclusion body myopathies (IBM). Several criteria and outcome measures have led to contradicting results. The investigators want to retrospectively assess the natural course of the disease in CCFDN and IBM patients according to the data recorded during clinical routine visits.

Clinical Trial Description

We wanted to assess the natural course in Congenital Cataract Facial Dysmorphism Neuropathy Syndrome (CCFDN) and sporadic and hereditary inclusion body myopathies (IBM) over 10 years to gain new insights in both conditions. ;

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Cataract
• Congenital Abnormalities
• Congenital Cataracts, Facial Dysmorphism, And Neuropathy
• Contracture
• Inclusion Body Myopathy, Autosomal-dominant
• Inclusion Body Myopathy, Autosomal-recessive
• Inclusion Body Myositis, Sporadic
• Muscular Diseases
• Myositis, Inclusion Body
• Ophthalmoplegia

• NCT number: NCT01902940
• Study type: Observational
• Source: Ludwig-Maximilians - University of Munich
• Status: Completed
• Phase: N/A
• Start date: June 2013
• Completion date: October 2013