共 50 条
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.
引用
收藏
页数:4
相关论文