Focal Dermal Hypoplasia (FDH), commonly known as Goltz Syndrome, is a rare genetic disorder primarily affecting females and characterized by a range of skin, skeletal, and ocular abnormalities.

Gorlin-Goltz syndrome (GS), also known as nevoid basal cell carcinoma syndrome, is an infrequent multisystem disease inherited in a dominant autosomal way, which shows a high level of penetrance and ...

Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is a rare condition characterised by skeletal abnormalities, odontogenic keratocysts and basal cell nevi. Diagnosis of this condition is ...

After amassing as much data as we could and with further literature search back to 1880, Bob Goltz and I wrote “Multiple Nevoid Basal Cell Epitheliomata, Jaw Cysts, Bifid Rib-a Syndrome ...