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.
Also Known As:
Syndrome, Goltz; Goltz's Syndrome; Goltz-Gorlin Syndrome; Dermal Hypoplasias, Focal; Focal Dermal Hypoplasias; Goltzs Syndrome; Gorlin Syndrome, Goltz; Hypoplasia, Focal Dermal; Hypoplasias, Focal Dermal; Syndrome, Goltz Gorlin; Syndrome, Goltz's; Syndrome, Goltz-Gorlin; Dermal Hypoplasia, Focal; Goltz Gorlin Syndrome; Goltz Syndrome