Evers M E, Steijlen P M, Hamel B C
Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
Clin Genet. 1995 Jun;47(6):295-301. doi: 10.1111/j.1399-0004.1995.tb03968.x.
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.