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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Egile Nagusiak: Sohini Banerjee (Egilea), Debkamal Kar (Egilea)
Formatua: Liburua
Argitaratua: Wolters Kluwer Medknow Publications, 2024-01-01T00:00:00Z.
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