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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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| Publicat a: | J Oral Maxillofac Pathol |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6421933/ https://ncbi.nlm.nih.gov/pubmed/30967739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jomfp.JOMFP_160_18 |
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