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Obstructive Jaundice Secondary to Ampullary Adenocarcinoma in Neurofibromatosis Type 1
Neurofibromatosis type 1 is an autosomal dominant genetic disorder with an estimated birth incidence of 1 in 3000–4000. The major diagnostic criterion includes multiple cutaneous neurofibromas, axillary or inguinal freckling, and café au lait spots. Gastrointestinal neoplasms have a reported occurre...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer India
2012
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3693330/ https://ncbi.nlm.nih.gov/pubmed/24426533 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12262-012-0513-9 |
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