IDENTIFICATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE I

$3,034M01FY2000RRNIH

University Of Pittsburgh At Pittsburgh, Pittsburgh PA

Investigators

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Abstract

The prospective investigation of families with multiple endocrine neoplasia 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 parathyroid glands. Patients with the syndrome have a diverse spectrum of initial presentation which has led to difficulty in understanding of the disorder.

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