Insights into Hyperparathyroidism-Jaw Tumour Syndrome: From Endocrine Acumen to the Spectrum of
CDC73
gene
hyperparathyroidism–jaw tumour syndrome
immunohistochemistry
jaw tumour
parafibromin
parathyroid carcinoma
parathyroid tumour
parathyroidectomy
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
15 Feb 2024
15 Feb 2024
Historique:
received:
19
12
2023
revised:
07
02
2024
accepted:
08
02
2024
medline:
24
2
2024
pubmed:
24
2
2024
entrez:
24
2
2024
Statut:
epublish
Résumé
A total of 1 out of 10 patients with primary hyperparathyroidism (PHP) presents an underlying genetic form, such as multiple endocrine neoplasia types 1, 2A, etc., as well as hyperparathyroidism-jaw tumour syndrome (HJT). We aimed to summarise the recent data, thus raising more awareness regarding HJT, from the clinical perspective of PHP in association with the challenges and pitfalls of
Identifiants
pubmed: 38396977
pii: ijms25042301
doi: 10.3390/ijms25042301
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Carol Davila University of Medicine and Pharmacy
ID : 2023