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A Multiple Endocrine Disorder

James H. Myers, MD; John J. Eversman, MD

Arch Intern Med. 1981;141(11):1521-1522.

Abstract
In the course of follow-up of a patient with primary hyperparathyroidism, signs and symptoms of acromegaly developed. The patient subsequently was found to have recurrent primary hyperparathyroidism and, later, pheochromocytoma was discovered. The patient seems to have an overlap of features found in the multiple endocrine neoplasia syndromes, type 1 and type 2 as previously classified.

(Arch Intern Med 1981;141:1521-1522)

Author Affiliations
From the Department of Endocrinology and Metabolism, the Cleveland Clinic Foundation and the Cleveland Clinic Educational Foundation.

Footnotes
Accepted for publication Nov 10, 1980.

Reprint requests to Department of Endocrinology and Metabolism, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44106 (Dr Eversman).

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