局灶性真皮发育不全（戈尔茨综合征）：病例报告。
Focal dermal hypoplasia (Goltz syndrome): case reports.
作者信息
Derks B, Gericke G S, Louw M
出版信息
S Afr Med J. 1978 Jul 1;54(1):27-9.
PMID:211652
Abstract
Two Cape Coloured children, both with physical stigmata of Goltz syndrome, are described. Accurate diagnosis of congenital defects in the newborn allows optimal planning of surgical treatment and more accurate prognosis and genetic counselling.
摘要
本文描述了两名患有戈尔茨综合征身体特征的开普混血儿童。对新生儿先天性缺陷的准确诊断有助于优化手术治疗方案，并能做出更准确的预后判断和遗传咨询。
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Focal dermal hypoplasia (Goltz syndrome): case reports.局灶性真皮发育不全（戈尔茨综合征）：病例报告。
S Afr Med J. 1978 Jul 1;54(1):27-9.
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