| Literature DB >> 7554362 |
M E Evers1, P M Steijlen, B C Hamel.
Abstract
We present an update of disorders in which aplasia cutis congenita is a feature. Localization of the lesion, important other features, and possible etiology are tabulated. Disorders are classified as chromosomal, monogenic, teratological/exogenous, and unknown. Points of particular interest in history taking and examination of patients with aplasia cutis congenita are presented.Entities:
Mesh:
Year: 1995 PMID: 7554362 DOI: 10.1111/j.1399-0004.1995.tb03968.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438