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Case Reports
. 1990 Aug;237(5):310-2.
doi: 10.1007/BF00314749.

"Quadriceps myopathy": a clinical variant form of Becker muscular dystrophy

Y Wada  1 , Y Itoh, T Furukawa, H Tsukagoshi, K Arahata
Affiliations
Case Reports

"Quadriceps myopathy": a clinical variant form of Becker muscular dystrophy

Y Wada et al. J Neurol. 1990 Aug.

Abstract

A 26-year-old male with "quadriceps myopathy" is presented. He had a family history and only the bilateral quadriceps were wasted, without symptomatic weakness. The specimen of the muscle biopsy showed typical myopathic features without inflammatory reactions. The patchy defect of muscular dystrophin was proved by immunohistochemical study. Dystrophin analysis revealed abnormal 380 kDa dystrophin. Gene deletion was proved at exon 45-48 of Xp21 without frameshift. This case was considered to be a clinical variant form of Becker muscular dystrophy.

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References

    1. Muscle Nerve. 1985 Jun;8(5):435-44 - PubMed
    1. Confin Neurol. 1958;18(6):416-41 - PubMed
    1. Cell. 1988 Aug 12;54(4):447-52 - PubMed
    1. Cell. 1987 Jul 31;50(3):509-17 - PubMed
    1. Nature. 1988 Jun 30;333(6176):861-3 - PubMed

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