Oral manifestations of multiple endocrine neoplasia 2B syndrome: A rare case report
Multiple endocrine neoplasia (MEN) 2B syndrome is a rare autosomal dominant hereditary condition of neuroendocrine origin characterized by pheochromocytoma, marfanoid habitus, and mucocutaneous neuromas. Multiple mucosal neuromas on the tongue, lips, cheeks, and inner eyelids are often appeared as t...
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Wolters Kluwer Medknow Publications,
2024-01-01T00:00:00Z.
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