| Literature DB >> 19616434 |
G Astrea1, J Schessl, E Clement, M Tosetti, E Mercuri, M Rutherford, G Cioni, C G Bönnemann, F Muntoni, R Battini.
Abstract
Reducing body myopathy is a rare progressive myopathy identified by characteristic pathological findings and secondary to dominantly acting mutations in the X-linked FHL1 gene. We report muscle MRI findings in two patients affected by reducing body myopathy and in their carrier mothers. All four showed a distinctive pattern of muscle alteration, with a predominant involvement of postero-medial muscle at thigh level and of soleus at calf level, with a striking sparing of glutei muscles that also appeared to be hypertrophic. These findings may help in the differential diagnosis of these disorders.Entities:
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Year: 2009 PMID: 19616434 DOI: 10.1016/j.nmd.2009.06.372
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296