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Small Bowel Diverticulosis and Jejunal Perforation in Marfan Syndrome
Marfan syndrome is an autosomal dominant disorder involving mutation in the FBN1 gene, which encodes fibrillin-1, a protein critical to maintain the integrity of connective tissue. A mutation in this gene can affect multiple organ systems, but it is not classically associated with gastrointestinal c...
Tallennettuna:
| Julkaisussa: | ACG Case Rep J |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American College of Gastroenterology
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5772063/ https://ncbi.nlm.nih.gov/pubmed/29392152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14309/crj.2018.5 |
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