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Familial nonmembranous aplasia cutis of the scalp. Pediatr Dermatol 2005 May-Jun;22(3):213-7 PMID: 15916567

Pubmed ID

15916567

Abstract

Aplasia cutis of the scalp is often a sporadic condition, but familial occurrences with an autosomal dominant inheritance have been documented. Aplasia cutis of the scalp may be seen in two main clinical variants: oval-shaped membranous aplasia cutis and irregular, larger defects. We report six families in whom more than one member has aplasia cutis of the scalp, all of them with large irregular defects located over the vertex or anterior to the vertex along the sagittal suture. We review previous reports of this entity with clinical pictures and note that in most instances, the defects are of the nonmembranous variant.

Author List

Baselga E, Torrelo A, Drolet BA, Zambrano A, Alomar A, Esterly NB

Author

Beth A. Drolet MD Professor in the Dermatology department at Medical College of Wisconsin




Scopus

2-s2.0-19644383976   19 Citations

MESH terms used to index this publication - Major topics in bold

Ectodermal Dysplasia
Female
Humans
Male
Scalp Dermatoses
jenkins-FCD Prod-300 626508253d14e4184314fb9f66322a03a5906796