Münchau A, Valente E M, Shahidi G A, Eunson L H, Hanna M G, Quinn N P, Schapira A H, Wood N W, Bhatia K P
Department of Clinical Neurology, Institute of Neurology, Queen Square, University College London, London WC1N 3BG, UK.
J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609.
To characterise the phenotype of a family with paroxysmal exercise induced dystonia (PED) and migraine and establish whether it is linked to the paroxysmal non-kinesigenic dyskinesia (PNKD) locus on chromosome 2q33-35, the familial hemiplegic migraine (FHM) locus on chromosome 19p, or the familial infantile convulsions and paroxysmal choreoathetosis (ICCA syndrome) locus on chromosome 16.
A family, comprising 30 members, was investigated. Fourteen family members in two generations including three spouses were examined. Haplotypes were reconstructed for all the available family members by typing several microsatellite markers spanning the PNKD, FHM, and ICCA loci. Additionally, the four exons containing the known FHM mutations were sequenced.
Of 14 members examined four were definitely affected and one member was affected by history. The transmission pattern in this family was autosomal dominant with reduced penetrance. Mean age of onset in affected members was 12 (range 9-15 years). Male to female ratio was 3:1. Attacks of PED in affected members were predominantly dystonic and lasted between 15 and 30 minutes. They were consistently precipitated by walking but could also occur after other exercise. Generalisation did not occur. Three of the affected members in the family also had migraine without aura. Linkage of the disease to the PNKD, FHM, or ICCA loci was excluded as no common haplotype was shared by all the affected members for each locus. In addition, direct DNA sequential analysis of the FHM gene (CACNL1A4) ruled out all known FHM point mutations.
This family presented with the classic phenotype of PED and is not linked to the PNKD, FHM, or ICCA loci. A new gene, possibly coding for an ion channel, is likely to be the underlying cause of the disease.
对一个患有阵发性运动诱发性肌张力障碍(PED)和偏头痛的家系进行表型特征分析,并确定其是否与2q33 - 35染色体上的阵发性非运动诱发性运动障碍(PNKD)基因座、19p染色体上的家族性偏瘫性偏头痛(FHM)基因座或16号染色体上的家族性婴儿惊厥和阵发性舞蹈手足徐动症(ICCA综合征)基因座相关。
对一个由30名成员组成的家系进行研究。检查了包括三名配偶在内的两代中的14名家庭成员。通过对跨越PNKD、FHM和ICCA基因座的几个微卫星标记进行分型,为所有可用的家庭成员重建单倍型。此外,对包含已知FHM突变的四个外显子进行测序。
在检查的14名成员中,4名确诊患病,1名成员有患病史而被认定患病。该家系的遗传模式为常染色体显性遗传,外显率降低。患病成员的平均发病年龄为12岁(范围9 - 15岁)。男女比例为3:1。患病成员的PED发作主要为肌张力障碍性,持续15至30分钟。发作总是由行走诱发,但也可能在其他运动后发生。未出现全身性发作。该家系中有3名患病成员也患有无先兆偏头痛。由于每个基因座的所有患病成员未共享共同单倍型,排除了该疾病与PNKD、FHM或ICCA基因座的连锁关系。此外,对FHM基因(CACNL1A4)的直接DNA序列分析排除了所有已知的FHM点突变。
这个家系呈现出PED的典型表型,且与PNKD、FHM或ICCA基因座无关。一种可能编码离子通道的新基因可能是该疾病的潜在病因。