Misleading localization by (18)F-fluorocholine PET/CT in familial hypocalciuric hypercalcemia type-3: a case report

BACKGROUND: Familial hypocalciuric hypercalcemia (FHH) is a heterogeneous autosomal-dominant disorder of calcium hemostasis that may be difficult to distinguish clinically from mild primary hyperparathyroidism. Loss-of-function mutations mainly involving Arg15 residue of the adaptor-related protein...

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Detalles Bibliográficos
Autores principales: Mukhtar, Noha N, Abouzied, Mohei El-Din M, Alqahtani, Mohammed H, Hammami, Muhammad M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836468/
https://www.ncbi.nlm.nih.gov/pubmed/33499837
http://dx.doi.org/10.1186/s12902-021-00683-z

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