Practical guidelines for DNA-based testing in multiple endocrine neoplasia type 1.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
C Larsson, M Nordenskjold, B Skogseid, K Oberg
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Abstract

Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant predisposition to neoplastic lesions of the parathyroid glands, the neuroendocrine pancreas, and the anterior pituitary gland. The predisposing genetic defect was localized to the long arm of chromosome 11 by genetic linkage analysis in three affected families. By analyzing six MEN 1 families with 14 DNA marker systems located close to the MEN 1 gene, we have developed a method to identify carriers of the MEN 1 predisposition. We describe practical aspects of such DNA-based diagnostic procedures.

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1型多发性内分泌肿瘤dna检测实用指南
多发性内分泌肿瘤1型(MEN 1)是一种常染色体显性易感性,可发生甲状旁腺、神经内分泌胰腺和垂体前叶的肿瘤病变。通过遗传连锁分析,将3个家族的易感遗传缺陷定位在11号染色体长臂上。通过分析6个具有14个靠近MEN 1基因的DNA标记系统的MEN 1家族,我们开发了一种识别MEN 1易感性携带者的方法。我们描述了这种基于dna的诊断程序的实际方面。
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Extracellular Ca2+ sensing in C-cells and parathyroid cells. Proceedings of the Urban Health Care Symposium II. June 2-4, 1991. Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Unusual features of multiple endocrine neoplasia. Long-term follow-up in four large MEN 2 families in The Netherlands.
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