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Article

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.

The Journal of clinical endocrinology and metabolism - 1 Jun 1998

Teh B T, Farnebo F, Twigg S, Höög A, Kytölä S, Korpi-Hyövälti E, Wong F K, Nordenström J, Grimelius L, Sandelin K, Robinson B, Farnebo L O, Larsson C

Abstract excerpt

Approximately 70 families with familial isolated hyperparathyroidism (FIHP) have been reported. Whether it is a separate entity or a variant of multiple endocrine neoplasia type 1 (MEN1 at 11q13) or hyperparathyroidism-jaw tumor (HPT-JT or HRPT2 at 1q21-32) syndrome is not known. We describe here 3 unreported families with familial primary hyperparathyroidism and evaluate their clinical, pathological, and genetic...

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Identifiers

PMID: 9626148
DOI: 10.1210/jcem.83.6.4896

Genes

MEN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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