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IDENTIFICATION OF FAMILIAL PHEOCHROMOCYTOMA OR VON HIPPEL LINDAU SYNDROME

IDENTIFICATION OF FAMILIAL PHEOCHROMOCYTOMA OR VON HIPPEL LINDAU SYNDROME
家族性嗜铬细胞瘤或冯·希佩尔·林道综合征的识别
批准号：
5218398
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/5218398
关键词：
brain disorders clinical research early diagnosis endocrine disorder diagnosis family genetics human subject multiple endocrine neoplasia neoplasm /cancer diagnosis nervous system disorder diagnosis neurofibromatosis pheochromocytoma retina disorder

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中文摘要
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英文摘要
The hypothesis to be tested in this study is that prospective investigation of families with an apparent excess of pheochromocytoma will allow earlier detection, syndrome delineation and improved outcome. Pheochromocytoma is a neoplasm of the adrenal medulla that is usually benign, sporad and unilateral, and such cases are not the subject of this protocol. Pheochromocytoma is occasionally one manifestation of inherited autosomal dominant endocrine/neurologic disorders. These include, but are not limited to MEN-IIa, MEN-IIb, Von Hippel-Lindau disease (VHL), and neurofibromatosis. The study, therefore, screens family members of probands for multiple 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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