Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated Hypercalcemia

Primary hyperparathyroidism (pHPT) is associated with familial syndromes such as multiple endocrine neoplasia type 1 (MEN1), 2A (MEN2A), MEN-like syndromes (CDKN1B), and CDC73-related disorder (hyperparathyroidism – jaw tumor syndrome (HPJT)). Familial hypocalciuric hypercalcemia (FHH) caused by CAS...

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Veröffentlicht in:Horm Cancer
Hauptverfasser: Khairi, Shafaq, Osborne, Jenae, Jacobs, Michelle F, Clines, Gregory T, Miller, Barbra S, Hughes, David T, Else, Tobias
Format: Artigo
Sprache:Inglês
Veröffentlicht: Springer US 2020
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Original Paper
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7945006/
https://ncbi.nlm.nih.gov/pubmed/32761341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12672-020-00394-2
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