Late-Onset Dystrophinopathy

被引:0
|
作者
Singh, Ranjan K. [1 ]
机构
[1] Dist Hosp, Antiretroviral Therapy Ctr, Internal Med, Khagaria, India
关键词
muscular dystrophy; maternal inheritance; dystrophin; duplication of exon; creatine kinase; DUCHENNE;
D O I
10.7759/cureus.20531
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dystrophinopathy is a spectrum of muscular dystrophies resulting from absolute to relative deficiency of dystrophin - a protein essential for muscle fiber integrity. This includes a severe form called Duchenne muscular dystrophy, a mild form called Becker muscular dystrophy, and intermediate muscular dystrophy. Becker muscular dystrophy relates to late-onset and slow progression muscle dystrophy caused by deletions or duplications in the dystrophin gene. Individuals with this type of tardive slow progression have a life expectancy of 60 years. A patient in his late 40s presented this disease with duplication of exon 2 in the dystrophin gene.
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页数:4
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