The hypothesis to be tested in this study is that prospective investigation of affected kindreds with MEN-IIa, MEN-IIb, or FMCT will allow early detection, syndrome delineation and improved survival. The polyendocrine neoplasms of MEN-II occur in two different inherited forms each with age-dependent biochemical and clinical penetrance: MEN type IIa (Sipple's syndrome) and MEN type IIb (multiple mucosal neurome syndrome). Medullary cancer of the thyroid (MCT), the most common index lesion of both MEN-IIa and MEN-IIb also occurs in a familial form, FMTC. This study, therefore, screens family members of probands for the potential expected endocrinopathy.

Project Start
Project End
Budget Start
Budget End
Support Year
35
Fiscal Year
1996
Total Cost
Indirect Cost
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