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

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 genetic alteration produced by a mutation in the “patched” tumor suppressor gene. This rare syndrome is characterized by bas...

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Detalles Bibliográficos
Autores principales: Sahu, Sudipto, Sahoo, Sushil, Banerjee, Rajarshi, Ghosh, Sucharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421933/
https://www.ncbi.nlm.nih.gov/pubmed/30967739
http://dx.doi.org/10.4103/jomfp.JOMFP_160_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421933/
https://www.ncbi.nlm.nih.gov/pubmed/30967739
http://dx.doi.org/10.4103/jomfp.JOMFP_160_18

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