A CASE OF FOCAL DERMAL HYPOPLASIA (GOLTZ SYNDROME) WITH SOME NEW ASPECTS
A CASE OF FOCAL DERMAL HYPOPLASIA (GOLTZ SYNDROME) WITH SOME NEW ASPECTS
复制标题
具有一些新表现的局灶性真皮发育不全（GOLTZ 综合征）一例
DOI：
--
复制
发表时间：
1977
期刊：
影响因子：
--
通讯作者：
E. Lommen
中科院分区：
文献类型：
--
作者：
N. Beganović;E. Lommen
摘要Beganović，N.和Lommcn，E.J.P.(荷兰埃因霍温圣约瑟夫齐肯赫伊斯儿科)。局灶性真皮发育不全1例(Goltz综合征)，并有一些新的表现。儿科学报，66：255,1977。-报告1例出生时诊断为局灶性皮肤发育不全(Goltz综合征)。报告了一些以前没有描述过的发现(半裂、腭裂和一条脐动脉缺失)。讨论了染色体显带技术研究中的正常发现。
Abstract Beganović, N. and Lommcn, E. J. P. (Paediatric Department, St. Josephziekenhuis, Eindhoven, the Netherlands). A case of focal dermal hypoplasia (Goltz syndrome), with some new aspects. Acta Paediatr Scand, 66:255, 1977.—A case of Focal Dermal Hypoplasia (Goltz syndrome), diagnosed at birth, is reported. Some findings not formerly described (hemimelia, schizis of the palatum molle and the absence of one umbilical artery) are reported. Normal findings in chromosome studies with banding techniques are discussed.