Dural ectasia accompanying a case of multiple endocrine neoplasia type 2B

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Multiple endocrine neoplasia type 2B in a Chinese patient.

Multiple endocrine neoplasia type 2B syndrome is rarely reported in Chinese patients. A 25-year-old Chinese male presented with full-blown clinical features of this syndrome, including bilateral phaeochromocytomas, medullary thyroid carcinoma, and characteristic phenotypic features. One-stage surgical treatment was performed and subsequent genetic analysis confirmed a point mutation at codon 91...

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A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract

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Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report

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A family presenting with multiple endocrine neoplasia type 2B: A case report

INTRODUCTION Multiple endocrine neoplasia 2B, a rare autosomal dominant syndrome, is characterized by early onset of medullary thyroid carcinoma, pheochromocytoma, marfanoid habitus and mucosal neuromas of the tongue, lips, inner cheeks and inner eyelids. Gangliomatosis of the gastrointestinal tract and its complications may also occur in patients with this disease. CASE PRESENTATION We prese...

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ژورنال

عنوان ژورنال: Endocrine Abstracts

سال: 2013

ISSN: 1479-6848

DOI: 10.1530/endoabs.32.p277