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Article

Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management.

Clinical endocrinology - 1 Feb 2006

Cetani Filomena, Pardi Elena, Ambrogini Elena, Lemmi Monica, Borsari Simona, Cianferotti Luisella, Vignali Edda, Viacava Paolo, Berti Piero, Mariotti Stefano, Pinchera Aldo, Marcocci Claudio

Abstract excerpt

OBJECTIVE: Familial isolated primary hyperparathyroidism (FIPH) can result from either incomplete expression of a syndromic form of familial primary hyperparathyroidism [multiple endocrine neoplasia type 1 (MEN 1), hyperparathyroidism-jaw tumour syndrome (HPT-JT) or familial hypocalciuric hypercalcaemia (FHH)] or still unrecognized causes. Design Genetic analyses of MEN1, HRPT2 and CASR genes in FIHP. PATIENTS:...

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Source

Identifiers

PMID: 16430712
DOI: 10.1111/j.1365-2265.2006.02438.x

Genes

MEN1
CASR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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