An enigma of Gorlin–Goltz syndrome: Two cases reported in mother and daughter

S Sahu, S Sahoo, R Banerjee… - Journal of Oral and …, 2019 - journals.lww.com
Gorlin–Goltz syndrome (GGS) also known as the nevoid basal cell carcinoma syndrome or
the nevus–Bifid rib syndrome is an inherited autosomal dominant syndrome. It is caused by …

Síndrome de Gorlin-Goltz-relato de casos

A Kuhn-Dall, O Rodrigo, L Jonathan, R Santos… - RFO …, 2014 - revodonto.bvsalud.org
Objetivo: este trabalho faz uma revisão de literatura sobre Síndrome de Gorlin-Goltz, citando
as diversas manifestações clínicas dessa síndrome, bem como, relata dois casos clínicos de …

Gorlin-Goltz syndrome in twin brothers: an unusual occurrence with review of the literature

S Anchlia, S Vyas, S Bahl, V Nagavadiya - Case Reports, 2015 - casereports.bmj.com
Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is caused by
genetic alteration produced by a mutation in the 'patched'tumour suppressor gene, and is …

Gorlin syndrome: A rare case report

S Shrivastava, S Nayak, P Nayak… - Journal of Oral and …, 2020 - journals.lww.com
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance
and variable expressivity. The syndrome is caused by mutations in PTCH, a tumor …

[PDF][PDF] Gorlin Goltz Syndrome: A Disease in Disguise

N Jain, AK Pillai, N Mishra, MD Ishtiyak… - … and Clinical Trials, 2022 - researchgate.net
Gorlin Goltz syndrome also known as nevoid basal cell carcinoma is an autosomal dominant
inherited disorder caused due to mutation in patched (PTCH) tumor suppressor gene …