We report three cases of aplasia cutis congenita of the scalp affecting two siblings and their mother, suggesting group 1, or autosomal dominant aplasia cutis congenita not associated with multiple abnormalities. A review of the clinical features and literature concerning this heterogenous and rare condition is presented.
This article is available only as a PDF. Please click on “Download PDF” on top to view the full article.
Declaration
The author(s) declare there are no affiliations with or involvement in any organisation or entity with any financial interest in the subject matter or materials discussed in this manuscript.
