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伴有先天性大理石样皮肤毛细血管扩张症的头皮和肢体缺损:亚当斯-奥利弗综合征?

Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome?

作者信息

Toriello H V, Graff R G, Florentine M F, Lacina S, Moore W D

机构信息

Blodgett Memorial Medical Center, Grand Rapids, Michigan.

出版信息

Am J Med Genet. 1988 Feb;29(2):269-76. doi: 10.1002/ajmg.1320290204.

Abstract

We report on a boy with congenital scalp and limb defects, consistent with a diagnosis of Adams-Oliver syndrome (aplasia cutis congenita with terminal transverse limb defects). An additional finding present in this child and in his mother was cutis marmorata telangiectatica congenita. Although this boy fits the diagnostic criteria for Adams-Oliver syndrome, his mother does not. We discuss whether this condition is highly variable, or heterogeneous.

摘要

我们报告了一名患有先天性头皮和肢体缺陷的男孩,符合亚当斯-奥利弗综合征(先天性皮肤发育不全伴肢体末端横向缺陷)的诊断。该患儿及其母亲还存在先天性网状青斑。虽然这个男孩符合亚当斯-奥利弗综合征的诊断标准,但他的母亲不符合。我们讨论了这种情况是高度可变还是异质性的。

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