Tertiary hyperparathyroidism in patients with pseudohypoparathyroidism type 1a

Pseudohypoparathyroidism type 1a (PHP1a) is a genetic disorder caused by heterozygous loss-of-function mutations on the maternal allele of the GNAS gene. Patients with PHP1a predominantly exhibit parathyroid hormone (PTH) resistance and physical features of Albright's hereditary osteodystrophy....

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Detalles Bibliográficos
Autores principales: Itoh, Masatsune, Okajima, Michiko, Kittaka, Yuko, Yachie, Akihiro, Wada, Taizo, Saikawa, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Full Length Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043659/
https://www.ncbi.nlm.nih.gov/pubmed/35497370
http://dx.doi.org/10.1016/j.bonr.2022.101569

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043659/
https://www.ncbi.nlm.nih.gov/pubmed/35497370
http://dx.doi.org/10.1016/j.bonr.2022.101569

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