Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysis.

We report the case of a 2-year-old girl who had signs of Duchenne type muscular dystrophy on clinical, electromyographic, laboratory, and pathological examination. The parents of the child are first cousins. A brother and nephew of the mother also had Duchenne type muscular dystrophy. Karyotype anal...

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Detaylı Bibliyografya
Asıl Yazarlar: Aymé, S, Pelissier, J F, Garnier, J M, Mattei, J F, Giraud, F
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1979
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1012617/
https://ncbi.nlm.nih.gov/pubmed/513086
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