Gillian Turner, Michael Partington, Bronwyn Kerr, Marie Mangelsdorf, Jozef Gecz
{"title":"在两个具有相同ARX基因突变的家庭中,智力低下、自闭症、癫痫和手部运动障碍的不同表达。","authors":"Gillian Turner, Michael Partington, Bronwyn Kerr, Marie Mangelsdorf, Jozef Gecz","doi":"10.1002/ajmg.10714","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":7708,"journal":{"name":"American Journal of Medical Genetics","volume":"112 4","pages":"405-11"},"PeriodicalIF":0.0000,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ajmg.10714","citationCount":"130","resultStr":"{\"title\":\"Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation.\",\"authors\":\"Gillian Turner, Michael Partington, Bronwyn Kerr, Marie Mangelsdorf, Jozef Gecz\",\"doi\":\"10.1002/ajmg.10714\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":7708,\"journal\":{\"name\":\"American Journal of Medical Genetics\",\"volume\":\"112 4\",\"pages\":\"405-11\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/ajmg.10714\",\"citationCount\":\"130\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Medical Genetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/ajmg.10714\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Medical Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/ajmg.10714","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 130
摘要
两个最初被诊断为非综合征性x连锁智力低下(NSXLMR)的家庭,在发现ARX基因有24bp重复(428- 451dup (24bp))后进行了回顾[Stromme et al., 2002: Nat Genet 30:441-445]。在其他三个家族中也发现了相同的重复:一个家族患有x连锁婴儿痉挛和心律失常(x连锁西综合征,MIM 308350),两个家族患有XLMR和手部张力障碍运动(帕廷顿综合征,MIM 309510)。回顾一下,在两个家庭的一些个体中都发现了韦斯特和帕廷顿综合征的表现。此外,还发现其中一人患有自闭症,两人有自闭症行为,其中一人患有癫痫。智力迟钝的程度从轻微到严重不等。GCG三核苷酸扩增(GCG)10+7和ARX基因1517 bp的缺失也被发现与West综合征和一个新发现的肌阵挛性癫痫、严重智力低下和痉挛性截瘫的家族中的错义突变(1058C>T)有关[Scheffer等人,2002:Neurology, in press]。显然,所有这些疾病都是同一基因突变的表现。婴儿痉挛、局灶性肌张力障碍、自闭症、癫痫和非综合征性智力低下患者的比例是由ARX基因突变引起的,这还有待观察。
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation.
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.