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缺指(趾)畸形与7号染色体长臂近端/中间间质缺失

Ectrodactyly and proximal/intermediate interstitial deletion 7q.

作者信息

McElveen C, Carvajal M V, Moscatello D, Towner J, Lacassie Y

机构信息

Department of Pediatrics, Louisiana State University Medical Center, New Orleans 70112, USA.

出版信息

Am J Med Genet. 1995 Mar 13;56(1):1-5. doi: 10.1002/ajmg.1320560102.

Abstract

We report on an individual with severe mental retardation, seizures, microcephaly, unusual face, scoliosis, and cleft feet and cleft right hand. The chromosomal study showed a proximal interstitial deletion 7q (q11.23q22). From our review of the literature, 11 patients have been reported with ectrodactyly (split hand/split foot malformation) and proximal/intermediate interstitial deletions or rearrangements of 7q. The critical segment for ectrodactyly seems to be located between 7q21.2 and 7q22.1. This malformation is present in 41% of the patients whose deletion involves the critical segment.

摘要

我们报告了一名患有严重智力发育迟缓、癫痫、小头畸形、面容异常、脊柱侧弯以及足裂和右手裂的个体。染色体研究显示存在7号染色体近端间质缺失(q11.23q22)。通过对文献的回顾,已有11例报告称患有裂手/裂足畸形(ectrodactyly)以及7号染色体近端/中间间质缺失或重排。裂手/裂足畸形的关键区段似乎位于7q21.2和7q22.1之间。在缺失涉及关键区段的患者中,41%存在这种畸形。

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