Retinal atrophy and MEN1 syndrome: case report

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Stambouli Roumeitha, Sifi Karima

Abstract

In this study, we present the case of a patient with multiple endocrine neoplasia type 1 (MEN1) syndrome. The patient presented with primary hyperparathyroidism (pHPT) which was associated with a microadenome in the right pole. This case presents additional complications related to an extensive
medical history of eye diseases and cancers in the family. Family medical history includes multiple cases of hyperparathyroidism and degenerative eye disease, as well as a previous death in the family due to metastases from another abdominal cancer.

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