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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 trac...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3287411/ https://ncbi.nlm.nih.gov/pubmed/22185228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-5-587 |
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