Aplasia cutis congenita and associated disorders: an update
- 1 June 1995
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 47 (6) , 295-301
- https://doi.org/10.1111/j.1399-0004.1995.tb03968.x
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.Keywords
This publication has 54 references indexed in Scilit:
- Pericardial agenesis and focal aplasia cutis in tetrasomy 12p (Pallister‐Killian syndrome)American Journal of Medical Genetics, 1992
- Johanson-Blizzard-SyndromKlinische Padiatrie, 1991
- Intrauterine herpes simplex infection resembling mechanobullous disease in a newborn infantJournal of the American Academy of Dermatology, 1986
- Aplasia cutis congenita: A clinical review and proposal for classificationJournal of the American Academy of Dermatology, 1986
- Aplasia cutis congenitaJournal of the American Academy of Dermatology, 1985
- Origin of scalp vertex aplasia cutisThe Journal of Pediatrics, 1982
- A new familial syndrome of 46,XY gonadal dysgenesis with anomalies of ectodermal and mesodermal structuresThe Journal of Pediatrics, 1980
- Aplasia cutis congenita: A cutaneous marker of occult spinal dysraphismThe Journal of Pediatrics, 1980
- Congenital absence of skinJournal of the American Academy of Dermatology, 1980
- The amniotic band disruption complex: Timing of amniotic rupture and variable spectra of consequent defectsPublished by Elsevier ,1979