A newborn with widespread skin lesions and extremity anomalies

被引：0

作者：

Isik, Dilek Ulubas ^{[1
]}

Ozcan, Beyza ^{[1
]}

Celik, Ulker ^{[1
]}

Aydemir, Ozge ^{[1
]}

Erdogan, Kadri Murat ^{[2
]}

Hekimoglu, Emre ^{[3
]}

Bas, Ahmet Yagmur ^{[1
]}

Demirel, Nihal ^{[1
]}

机构：

[1] Etlik Zubeyde Hanim Womens Hlth Teaching & Res Ho, Dept Neonatol, Neonatal Intens Care Unit, TR-06010 Ankara, Turkey

[2] Etlik Zubeyde Hanim Womens Hlth Teaching & Res Ho, Dept Genet, TR-06010 Ankara, Turkey

[3] Etlik Zubeyde Hanim Womens Hlth Teaching & Res Ho, Dept Ophthalmol, TR-06010 Ankara, Turkey

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 2014年 / 173卷 / 04期

关键词：

Extremity anomalies; Focal dermal hypoplasia; Newborn;

D O I：

10.1007/s00431-013-2195-0

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A variety of diseases can cause vesicular or pustular eruptions in newborns. A thorough clinical history and physical exam provide important clues for differential diagnosis. Goltz syndrome, also known as focal dermal hypoplasia, is a rare genodermatosis and generally diagnosed by the presence of the characteristic skin lesions. We present an infant with aplasia cutis, atrophic skin lesions, syndactyly and eye abnormalities who was diagnosed with Goltz syndrome soon after birth. Goltz syndrome should be considered in differential diagnosis of hypoplastic or aplastic skin lesions in neonates in the presence of skeletal or ophthalmic anomalies.

引用

页码：545 / 546

页数：2