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A multidisciplinary approach to the successful management of Gorlin syndrome
Gorlin–Goltz syndrome (GGS) is a rare genetic syndrome with variable expressivity and autosomal dominant inheritance. The major features of GGS include numerous basal cell carcinomas (BCCs), keratocysts of the jaw, palmar/plantar pits and calcification of the falx cerebri. Authors report the case of...
Guardat en:
| Publicat a: | J Surg Case Rep |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5460005/ https://ncbi.nlm.nih.gov/pubmed/28616153 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jscr/rjw224 |
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