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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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:ACG Case Rep J
Prif Awduron: Robey, Benjamin S., Peery, Anne F., Dellon, Evan S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American College of Gastroenterology 2018
Pynciau:
Mynediad Ar-lein: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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