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J Am Acad Dermatol ; 32(2 Pt 2): 315-8, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7829732

ABSTRACT

We observed a newborn infant of a previously reported kindred with absent dermal ridge pattern, syndactyly, and facial milia. The infant's features were consistent with three other kindreds, suggesting that this entity is a single disorder with variable expression. Furthermore, this entity should be considered in the differential diagnosis of excessive congenital facial milia and erosions.


Subject(s)
Epidermal Cyst/congenital , Epidermal Cyst/genetics , Facial Dermatoses/congenital , Facial Dermatoses/genetics , Skin Abnormalities , Syndactyly/genetics , Adult , Female , Foot Dermatoses/congenital , Foot Dermatoses/genetics , Hand Dermatoses/congenital , Hand Dermatoses/genetics , Humans , Infant, Newborn , Male , Nail Diseases/congenital , Nail Diseases/genetics , Pedigree
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