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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Main Authors: Sohini Banerjee (Author), Debkamal Kar (Author)
Formato: Livro
Publicado em: Wolters Kluwer Medknow Publications, 2024-01-01T00:00:00Z.
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3rd Floor Main Library

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