[Severe bone complications of primary hyperparathyroidism in a young patient with the rare verified mutation of MEN1].

Abstract excerpt

Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine tumors. Unfortunately, none of the described MEN1 mutations has been associated with a peculiar clinical phenotype, even within members of the same family, thus a genotype-to-phenotype correlation does not exist. MEN1 syndrome is the most common cause of...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Hyperparathyroidism, Primary
• Share to Hyperplasia