Add to ORKGGorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expressivity. It is characterized by facial dysmorphism, skeletal anomalies, multiple basal cell carcinomas, odontogenic keratocysts (OKC), palmar and plantar pits, bifid ribs, vertebral anomalies and a variety of other malformations. Various neoplasms', such as medulloblastomas, meningiomas, ovarian and cardiac fibromas are also found in this syndrome. Objective: To describe a twelve-year-old patient with Gorlin-Goltz syndrome, with basal cell carcinomas and promyelocytic leukemia developed after receiving craniospinal radiation for a medulloblastoma. Mild ribs as well as mandibular and maxillar OKC were also diagnosed. Conclusion: The patient wit...
Gorlin-Goltz syndrome (GGS) also known as Nevoid Basal Cell Carcinoma Syndrome is a rare autosomal-d...
Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder with a high degree of penetrance and v...
PubMedID: 25818966Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal domina...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
Gorlin-Goltz syndrome (SGG) is a rare autosomal dominant disorder. Although it is hereditary, there ...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent mu...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinoma...
Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with compl...
Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized b...
Copyright © 2014 Yeliz Bilir et al.This is an open access article distributed under theCreative Comm...
Gorlin and Goltz syndrome are a very complex syndrome and a multisystemic process that is characteri...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
Gorlin-Goltz syndrome (GGS) also known as Nevoid Basal Cell Carcinoma Syndrome is a rare autosomal-d...
Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder with a high degree of penetrance and v...
PubMedID: 25818966Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal domina...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
Gorlin-Goltz syndrome (SGG) is a rare autosomal dominant disorder. Although it is hereditary, there ...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent mu...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinoma...
Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with compl...
Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized b...
Copyright © 2014 Yeliz Bilir et al.This is an open access article distributed under theCreative Comm...
Gorlin and Goltz syndrome are a very complex syndrome and a multisystemic process that is characteri...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
Gorlin-Goltz syndrome (GGS) also known as Nevoid Basal Cell Carcinoma Syndrome is a rare autosomal-d...
Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder with a high degree of penetrance and v...
PubMedID: 25818966Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal domina...