Case Report: Papillary thyroid carcinoma in Goltz–Gorlin syndrome

Goltz–Gorlin syndrome (GGS), also known as focal dermal hypoplasia, is a rare X-linked disorder caused by pathogenic variants in the PORCN gene and characterized by several abnormalities, including skin and limb defects, papillomas in multiple organs, ocular malformations, and mild facial dysmorphis...

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Detalles Bibliográficos
Autores principales: Costanza, Flavia, Papi, Giampaolo, Corrado, Stefania, Pontecorvi, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582693/
https://www.ncbi.nlm.nih.gov/pubmed/37859990
http://dx.doi.org/10.3389/fendo.2023.1243540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582693/
https://www.ncbi.nlm.nih.gov/pubmed/37859990
http://dx.doi.org/10.3389/fendo.2023.1243540

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