A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.
Synonyms: Focal Dermal Hypoplasia Dermal Hypoplasia, Focal Hypoplasias, Focal Dermal Goltz-Gorlin Syndrome Syndrome, Goltz Gorlin Goltz's Syndrome Gorlin Syndrome, Goltz Syndrome, Goltz's Goltz Gorlin Syndrome Goltz Syndrome Syndrome, Goltz-Gorlin Syndrome, Goltz Goltzs Syndrome Focal Dermal Hypoplasias Hypoplasia, Focal Dermal Dermal Hypoplasias, Focal
Term information
91(85); was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92
91; was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92
do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME
use FOCAL DERMAL HYPOPLASIA to search GOLTZ-GORLIN SYNDROME 1985-92