Turner Gillian, Partington Michael, Kerr Bronwyn, Mangelsdorf Marie, Gecz Jozef
Hunter Genetics and the University of Newcastle, Waratah, NSW, Australia.
Am J Med Genet. 2002 Nov 1;112(4):405-11. doi: 10.1002/ajmg.10714.
Two families, originally diagnosed as having nonsyndromic X-linked mental retardation (NSXLMR), were reviewed when it was shown that they had a 24-bp duplication (428-45 1dup(24bp)) in the ARX gene [Stromme et al., 2002: Nat Genet 30:441-445]. This same duplication had also been found in three other families: one with X-linked infantile spasms and hypsarrhythmia (X-linked West syndrome, MIM 308350) and two with XLMR and dystonic movements of the hands (Partington syndrome, MIM 309510). On review, manifestations of both West and Partington syndromes were found in some individuals from both families. In addition, it was found that one individual had autism and two had autistic behavior, one of whom had epilepsy. The degree of mental retardation ranged from mild to severe. A GCG trinucleotide expansion (GCG)10+7 and a deletion of 1,517 bp in the ARX gene have also been found in association with the West syndrome, and a missense mutation (1058C>T) in a family with a newly recognized form of myoclonic epilepsy, severe mental retardation, and spastic paraplegia [Scheffer et al., 2002: Neurology, in press]. Evidently all these disorders are expressions of mutations in the same gene. It remains to be seen what proportions of patients with infantile spasms, focal dystonia, autism, epilepsy, and nonsyndromic mental retardation are accounted for by mutations in the ARX gene.
最初被诊断为患有非综合征性X连锁智力迟钝(NSXLMR)的两个家族,在发现他们的ARX基因存在一个24碱基对的重复(428 - 451dup(24bp))时,接受了重新评估[斯特罗姆等人,2002年:《自然遗传学》30卷:441 - 445页]。在其他三个家族中也发现了同样的重复:一个家族患有X连锁婴儿痉挛症和高峰节律紊乱(X连锁韦斯特综合征,MIM 308350),另外两个家族患有XLMR和手部张力障碍性运动(帕廷顿综合征,MIM 309510)。重新评估时,在这两个家族的一些个体中发现了韦斯特综合征和帕廷顿综合征的表现。此外,还发现一名个体患有自闭症,两名个体有自闭症行为,其中一人患有癫痫。智力迟钝的程度从轻度到重度不等。在与韦斯特综合征相关的研究中还发现了ARX基因中的一个GCG三核苷酸扩展(GCG)10 + 7以及1517碱基对的缺失,并且在一个患有新认识的肌阵挛性癫痫、严重智力迟钝和痉挛性截瘫的家族中发现了一个错义突变(1058C>T)[谢弗等人,2002年:《神经病学》,即将发表]。显然,所有这些疾病都是同一基因突变的表现。婴儿痉挛症、局灶性肌张力障碍、自闭症、癫痫和非综合征性智力迟钝患者中,由ARX基因突变导致的比例还有待确定。