A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes.

O'Halloran, D J; Shalet, S M · J Clin Endocrinol Metab · 1994

case_report · Level V

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Abstract

The multiple endocrine neoplasia (MEN) type 1 and McCune-Albright syndromes share many clinical and biochemical characteristics. This report documents for the first time the occurrence and natural history of the McCune-Albright syndrome in a female with a strong family history of MEN type 1. There may be a functional link between both of these conditions, and there is a need to look for G-protein mutations as a mechanism for disease in MEN type 1.

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