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同胞中先天性皮肤发育不全合并肢体、眼部及脑部异常:亚当斯-奥利弗综合征的一种变异型?

Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?

作者信息

Orstavik K H, Strömme P, Spetalen S, Flage T, Westvik J, Vesterhus P, Skjeldal O

机构信息

Department of Medical Genetics, Ullevål University Hospital, Oslo, Norway.

出版信息

Am J Med Genet. 1995 Oct 23;59(1):92-5. doi: 10.1002/ajmg.1320590118.

Abstract

Aplasia cutis congenita (ACC) may occur in isolation or with other congenital malformations. Peripheral limb anomalies and ACC are major elements of the Adams-Oliver syndrome, which is usually inherited as an autosomal dominant disorder. We report on a sister and brother with ACC and brain, eyes, and transverse limb anomalies. The phalanges of the hands and feet were either short or absent. The girl also had absence of right patella, was severely mentally retarded and blind with retinal nonattachment. The boy had a falciform fold in the left eye. He died at age one week and autopsy showed partial agenesis of corpus callosum. The findings in the sibs may represent a severe variant of the Adams-Oliver syndrome, or a previously unrecognized syndrome involving vascular disruption.

摘要

先天性皮肤发育不全(ACC)可单独出现或伴有其他先天性畸形。肢体周围异常和ACC是亚当斯-奥利弗综合征的主要组成部分,该综合征通常作为常染色体显性疾病遗传。我们报告了一对患有ACC以及脑、眼和四肢横向异常的兄妹。手足的指骨要么短小要么缺失。女孩还没有右髌骨,严重智力发育迟缓且因视网膜脱离而失明。男孩左眼有镰状皱襞。他在一周龄时死亡,尸检显示胼胝体部分发育不全。这对兄妹的发现可能代表亚当斯-奥利弗综合征的一种严重变体,或者是一种以前未被认识的涉及血管破坏的综合征。

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