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短肋发育不全组(伴/不伴多指畸形):1例患者报告提示存在连续谱系。

Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum.

作者信息

Franceschini P, Guala A, Vardeu M P, Signorile F, Franceschini D, Bolgiani M P

机构信息

Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Chivasso, Italy.

出版信息

Am J Med Genet. 1995 Nov 20;59(3):359-64. doi: 10.1002/ajmg.1320590316.

Abstract

We report on a patient with manifestations typical of Mohr syndrome and of the short rib (polydactyly) syndromes (SR(P)S) Majewski, Verma-Naumoff, Beemer, and Jeune. It seems possible that the different types of SR(P) syndromes, rather than being distinct conditions, are part of a large disease spectrum. The frequent overlap between orofaciodigital syndromes and SR(P) syndromes may be interpreted as the outcome of deletions of different size within the same chromosome region.

摘要

我们报告了一名患有典型莫尔综合征以及短肋(多指)综合征(SR(P)S)(马耶夫斯基型、韦尔马 - 瑙莫夫型、比默型和热内型)临床表现的患者。不同类型的SR(P)综合征似乎并非是截然不同的病症,而是一个大疾病谱的一部分。口面指综合征与SR(P)综合征之间频繁的重叠现象,可能被解释为同一染色体区域内不同大小缺失的结果。

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