Finlay A Y, Marks R
Br J Dermatol. 1978 Oct;99(4):423-30. doi: 10.1111/j.1365-2133.1978.tb06182.x.
A syndrome, consisting of a congenital abnormality of the scalp, ears and nipples inherited as an autosomal dominant trait, is reported. Ten affected members of a family over five generations are recorded and the four living affected members are described in detail. A review of congenital localized aplasias of skin suggests that this may be a new syndrome.