Malapert D, Recan D, Leturcq F, Degos J D, Gherardi R K
Département de Neurosciences, Centre Hospitalo-Universitaire Henri Mondor, Créteil, France.
J Neurol Neurosurg Psychiatry. 1995 Nov;59(5):552-4. doi: 10.1136/jnnp.59.5.552.
A 25 year old woman, without family history of muscular dystrophy, had had an isolated lower limb hypertrophy since infancy and later experienced exercise-induced myalgia. Genomic DNA analysis showed a deletion of exons 45 to 52 of the dystrophin gene. Uncommon phenotypes of dystrophinopathies and consequences in genetic counselling in women are emphasised.
一名25岁女性,无肌营养不良家族史,自婴儿期起出现孤立性下肢肥大,后来经历运动诱发的肌痛。基因组DNA分析显示肌营养不良蛋白基因外显子45至52缺失。强调了肌营养不良病的罕见表型以及对女性遗传咨询的影响。