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IDENTIFICATION OF PATIENTS WITH FAMILIAL PHEOCHROMOCYTOMA/VON HIPPLE LINDAU SYN

IDENTIFICATION OF PATIENTS WITH FAMILIAL PHEOCHROMOCYTOMA/VON HIPPLE LINDAU SYN
家族性嗜铬细胞瘤/VON HIPPLE LINDAU SYN 患者的识别
批准号：
6114599
负责人：
SALLY CARTY
金额：
$2.9万
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：
--
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/6114599
关键词：
adrenal medulla neoplasm autosomal dominant trait brain neoplasms clinical research eye neoplasms family genetics genetic disorder diagnosis human subject neoplasm /cancer diagnosis nervous system neoplasms pheochromocytoma

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英文摘要
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, sporadic 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.
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IDENTIFICATION OF PATIENTS W/ FAMILIAL HYPOCALCIURIC HYPERCALCEMIA
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