Chudley A E, Tackels D C, Lubs H A, Arena J F, Stoeber W P, Kovnats S, Stevenson R E, Schwartz C E
Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada.
Am J Med Genet. 1999 Jul 30;85(3):255-62. doi: 10.1002/(sici)1096-8628(19990730)85:3<255::aid-ajmg14>3.0.co;2-z.
We identified a family with three males in two generations with moderate mental retardation. The two oldest were first cousins whose mothers were sisters. The third affected was a grandson through a daughter of one of the sisters, strongly suggesting X- linked inheritance. The affected males had prominent glabella, synophrys, prognathism, generalized hirsutism, and bilateral single palmar creases. All developed seizures in childhood. The two oldest have had a slow deterioration in neurological status with poor gait and balance and progressive weakness. No deterioration in their mental status has been observed. The oldest had cerebellar atrophy confirmed on computed tomography and magnetic resonance imaging scans of the brain and prolonged nerve conduction velocity. Two of the males had hypogammaglobulinemia (IgA deficient). Two-point linkage analysis using 27 microsatellite markers on the X chromosome resulted in a maximum LOD score of 2.23 at straight theta = 0 for locus DSX101. Recombination was observed at locus DSX1170 in Xq21.33 and locus DXS8067 in Xq23. We conclude that this family represents an X-linked disorder associated with a recognizable phenotype, progressive neurological deterioration, and variable hypogammaglobulinemia. The gene appears to lie between Xq21.33 and Xq23.
我们鉴定出一个家族,两代中有三名男性患有中度智力迟钝。年龄较大的两人是表亲,他们的母亲是姐妹。第三名患者是其中一名姐妹的女儿所生的外孙,这强烈提示为X连锁遗传。患病男性眉间突出、眉连、凸颌、全身多毛,且有双侧单掌褶。所有人在儿童期均出现癫痫发作。年龄较大的两人神经功能状况逐渐恶化,步态和平衡差,且逐渐出现无力。未观察到他们的精神状态恶化。年龄最大者经脑部计算机断层扫描和磁共振成像扫描证实有小脑萎缩,神经传导速度延长。两名男性有低丙种球蛋白血症(IgA缺乏)。使用X染色体上的27个微卫星标记进行两点连锁分析,在基因座DSX101处,当θ = 0时,最大对数优势分数为2.23。在Xq21.33的基因座DSX1170和Xq23的基因座DXS8067处观察到重组。我们得出结论,这个家族代表一种与可识别的表型、进行性神经功能恶化和可变的低丙种球蛋白血症相关的X连锁疾病。该基因似乎位于Xq21.33和Xq23之间。