(18)F-FDG PET/CT and Whole-Body Bone Scan Findings in Gorlin–Goltz Syndrome

Gorlin–Goltz syndrome (basal cell nevus syndromes) is an uncommon, autosomal dominant inherited disorder characterized by developing basal cell carcinomas from a young age. Other distinct clinical features include keratocystic odontogenic tumors, dyskeratotic palmar and plantar pitting, and skeletal...

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Detalles Bibliográficos
Autores principales: Cheon, Miju, Yoo, Jang, Kang, Kyu-Bok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340262/
https://www.ncbi.nlm.nih.gov/pubmed/37443633
http://dx.doi.org/10.3390/diagnostics13132239

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340262/
https://www.ncbi.nlm.nih.gov/pubmed/37443633
http://dx.doi.org/10.3390/diagnostics13132239

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