Hyperparathyroidism-jaw tumour syndrome

被引：93

作者：

Chen, JD

Morrison, C

Zhang, C

Kahnoski, K

Carpten, JD

Teh, BT

机构：

[1] Van Andel Res Inst, Canc Genet Lab, Grand Rapids, MI 49503 USA

[2] Ohio State Univ, Dept Pathol, Ctr Comprehens Canc, Columbus, OH 43210 USA

[3] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA

来源：

JOURNAL OF INTERNAL MEDICINE | 2003年 / 253卷 / 06期

关键词：

HRPT2; hyperparathyroidism; jaw tumour; Parafibromin;

D O I：

10.1046/j.1365-2796.2003.01168.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Amongst hyperparathyroidism-related syndromes, hyperparathyroidism-jaw tumour syndrome is one of the least common and relatively unknown but its clinical and genetic aspects are not less interesting or important. With the recent identification of its genes, we can now better characterize the disease, both clinically and genetically, which will certainly impact the field of endocrinology and oncology. In this article, we review the clinico-pathological features and genetic basis of this syndrome with the hope that it will create awareness and interest in this disease amongst clinicians and basic scientists.

引用

页码：634 / 642

页数：9

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