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GTR Home > Conditions/Phenotypes > Distal myopathy with anterior tibial onset

Summary

A rare genetic neuromuscular disease with characteristics of a progressive muscle weakness starting in the anterior tibial muscles, later involving lower and upper limb muscles, associated with an increased serum creatine kinase levels and absence of dysferlin on muscle biopsy. There is evidence the disease is caused by homozygous mutation in the gene encoding dysferlin (DYSF) on chromosome 2p13. Patients become wheelchair dependent. [from SNOMEDCT_US]

Available tests

37 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: FER1L1, LGMD2B, LGMDR2, MMD1, DYSF
    Summary: dysferlin

Clinical features

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