Case Reports
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy
- PMID: 3742857
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Case Reports
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy
Clin Genet.
1986 Jun.
Abstract
An isolated case of Duchenne muscular dystrophy in a 15-year-old retarded girl with a de novo t(X;2) (p21.2;q37) translocation is described. Her clinical history is presented, with particular emphasis on CK level determinations made at several different times during her development. The similarities between this patient and previously reported females with Duchenne muscular dystrophy are discussed with reference to de novo translocations with a breakpoint at Xp21 and the risk of DMD in such females.
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