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IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE I

IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE I
I 型多发性内分泌肿瘤患者的识别
批准号：
5218396
负责人：
SALLY CARTY
金额：
$0.0万
依托单位：
--
依托单位国家：
美国
项目类别：
财政年份：
--
资助国家：
美国
项目状态：
未结题
起止时间：
至
来源：
https://reporter.nih.gov/project-details/5218396
关键词：
clinical research early diagnosis endocrine disorder diagnosis family genetics human subject multiple endocrine neoplasia neoplasm /cancer diagnosis

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英文摘要
The hypothesis to be tested in this study is that prospective investigation of families with MEN I will allow early detection, syndrome delineation, and improved outcome. MEN-I is an autosomal dominant inherited disorder of dysplasia of the anterior pituitary gland, the islet cell of the pancreas and the parathyroid glands. Patients with the syndrome have a diverse spectrum of initial presentation which has led to significant understanding of the disorder. Although MEN-I is expressed with high penetrance, at diagnosis most patients have symptoms of only one endocrinopathy or are asymptomatic. This study, therefore, screens family members of patients for a variety of endocrinopathies.
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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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