Kamm Christoph, Mayer Petra, Sharma Manu, Niemann Gerhard, Gasser Thomas
Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany.
Mov Disord. 2007 Apr 30;22(6):873-7. doi: 10.1002/mds.21350.
To date, there are few reports of paroxysmal exercise-induced dystonia associated with familial epilepsy. We describe a family with 4 affected members spanning 3 generations, suggestive of autosomal-dominant inheritance, who exhibited typical exercise-induced dystonia, different types of epilepsy (absence and primary generalized seizures), developmental delay, and migraine in variable combinations. Linkage of the disease to loci on chromosome 2 (paroxysmal nonkinesigenic dyskinesia) and chromosome 16 (paroxysmal kinesigenic choreoathetosis, infantile convulsions with choreoathetosis) was excluded, suggesting an as yet unidentified underlying genetic basis.
迄今为止,关于阵发性运动诱发性肌张力障碍伴发家族性癫痫的报道很少。我们描述了一个三代中有4名受累成员的家族,提示常染色体显性遗传,他们表现出典型的运动诱发性肌张力障碍、不同类型的癫痫(失神发作和原发性全身性发作)、发育迟缓以及偏头痛等不同症状组合。该疾病与2号染色体上的位点(阵发性非运动诱发性运动障碍)和16号染色体上的位点(阵发性运动诱发性舞蹈手足徐动症、伴有舞蹈手足徐动症的婴儿惊厥)的连锁关系被排除,这表明存在尚未明确的潜在遗传基础。