首页> 美国卫生研究院文献>American Journal of Human Genetics >Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region WHSCR-2
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Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region WHSCR-2

机译:在当前公认的WHS关键区域之外绘制Wolf-Hirschhorn综合征表型并定义新的关键区域WHSCR-2

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摘要

In an attempt to define the distinctive Wolf-Hirschhorn syndrome (WHS) phenotype, and to map its specific clinical manifestations, a total of eight patients carrying a 4p16.3 microdeletion were analyzed for their clinical phenotype and their respective genotypes. The extent of each individual deletion was established by fluorescence in situ hybridization, with a cosmid contig spanning the genomic region from MSX1 (distal half of 4p16.1) to the subtelomeric locus D4S3359. The deletions were 1.9–3.5 Mb, and all were terminal. All the patients presented with a mild phenotype, in which major malformations were usually absent. It is worth noting that head circumference was normal for height in two patients (those with the smallest deletions [1.9 and 2.2 Mb]). The currently accepted WHS critical region (WHSCR) was fully preserved in the patient with the 1.9-Mb deletion, in spite of a typical WHS phenotype. The deletion in this patient spanned the chromosome region from D4S3327 (190 b4 cosmid clone included) to the telomere. From a clinical point of view, the distinctive WHS phenotype is defined by the presence of typical facial appearance, mental retardation, growth delay, congenital hypotonia, and seizures. These signs represent the minimal diagnostic criteria for WHS. This basic phenotype maps distal to the currently accepted WHSCR. Here, we propose a new critical region for WHS, and we refer to this region as “WHSCR-2.” It falls within a 300–600-kb interval in 4p16.3, between the loci D4S3327 and D4S98-D4S168. Among the candidate genes already described for WHS, LETM1 (leucine zipper/EF-hand-containing transmembrane) is likely to be pathogenetically involved in seizures. On the basis of genotype-phenotype correlation analysis, dividing the WHS phenotype into two distinct clinical entities, a “classical” and a “mild” form, is recommended for the purpose of proper genetic counseling.
机译:为了定义独特的Wolf-Hirschhorn综合征(WHS)表型并绘制其特定的临床表现,共对8位携带4p16.3微缺失的患者进行了临床表型和各自基因型分析。通过荧光原位杂交确定每个单个缺失的程度,粘粒重叠群跨越从MSX1(4p16.1的远端一半)到亚端粒基因座D4S3359的基因组区域。缺失为1.9–3.5 Mb,且全部为末端。所有患者均表现为轻度表型,通常不存在主要畸形。值得注意的是,两名患者的身高在头围正常(缺失最小的患者[1.9和2.2 Mb])。尽管有典型的WHS表型,但目前接受的WHS关键区域(WHSCR)在具有1.9-Mb缺失的患者中已完全保留。该患者的缺失跨越了从D4S3327(包括190 b4粘粒克隆)到端粒的染色体区域。从临床角度来看,独特的WHS表型由典型的面部外观,智力低下,生长迟缓,先天性肌张力减退和癫痫发作的存在定义。这些标志代表了WHS的最低诊断标准。该基本表型位于当前接受的WHSCR的远端。在此,我们为WHS提出了一个新的关键区域,我们将该区域称为“ WHSCR-2”。它位于位点D4S3327和D4S98-D4S168之间的4p16.3的300-600kb区间内。在已经针对WHS进行描述的候选基因中,LETM1(亮氨酸拉链/含EF手的跨膜)很可能与癫痫病有关。基于基因型与表型的相关性分析,建议将WHS表型分为两个不同的临床实体,即“经典”和“轻度”两种形式,以进行适当的遗传咨询。

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