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IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA AND IIB

IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA AND IIB
IIA 型和 IIB 型多发性内分泌肿瘤患者的识别
批准号：
6219198
负责人：
SALLY CARTY
金额：
$0.3万
依托单位：
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
依托单位国家：
美国
项目类别：
财政年份：
1998
资助国家：
美国
项目状态：
已结题
起止时间：
1998-12-01 至 1999-11-30
来源：
https://reporter.nih.gov/project-details/6219198
关键词：
clinical research early diagnosis endocrine disorder diagnosis family genetics human subject multiple endocrine neoplasia neoplasm /cancer diagnosis

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中文摘要
翻译
本研究中检验的假设是，对多发性内分泌瘤（MEN）-IIa、MEN-IIb或FMCT受影响的运动的前瞻性研究将允许早期检测、综合征描述和改善生存率。MEN-II的多内分泌肿瘤以2种不同的遗传形式发生，每种遗传形式具有年龄依赖性生化和临床特征：MEN IIa型（Sipple综合征）和MEN IIb型（多粘液神经瘤综合征）。甲状腺髓样癌（MCT）是两种类型中最常见的索引病变。
英文摘要
The hypothesis tested in this study is that prospective investigation of affected kindreds with multiple endocrine neoplasia (MEN)-IIa, MEN-IIb or FMCT will allow early detection, syndrome delineation & improved survival. The poly-endocrine neoplasms of MEN-II occur in 2 different inherited forms each with age dependent biochemical & clinical penetrance: MEN type IIa (Sipple's Syndrome) & MEN type IIb (multimucosal neurome syndrome). Medullary cancer of the thyroid (MCT) is the most common index lesion of both types.
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IDENTIFICATION OF PATIENTS W/ FAMILIAL HYPOCALCIURIC HYPERCALCEMIA
IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE I
IDENTIFICATION OF PATIENTS W/ FAMILIAL HYPOCALCIURIC HYPERCALCEMIA
IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE I
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