Mevalonate kinase deficiency and IBD: shared genetic background
- PMID: 24531851
- PMCID: PMC4112436
- DOI: 10.1136/gutjnl-2013-306555
Mevalonate kinase deficiency and IBD: shared genetic background
Keywords: Gene Mutation; Genetic Polymorphisms; Inflammatory Bowel Disorders; Intestinal Gene Regulation; Molecular Genetics.
Comment on
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Monogenic diseases associated with intestinal inflammation: implications for the understanding of inflammatory bowel disease.Gut. 2013 Dec;62(12):1795-805. doi: 10.1136/gutjnl-2012-303956. Gut. 2013. PMID: 24203055 Review.
References
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- Uhlig HH. Monogenic diseases associated with intestinal inflammation: implications for the understanding of inflammatory bowel disease. Gut 2013;62:1795–805 - PubMed
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- Patra KP, Dariya V, Thomas W, et al. Index of suspicion: case 1: leg cramps, hand spasms, diarrhea, and substantial weight loss in a 12 year old: case 2: hypothermia, hypoglycemia, and hyperbilirubinemia in a neonate: case 3: recurrent fevers, abdominal pain, and cervical lymphadenopathy in a 7 year old. Pediatr Rev 2011;32:299–305 - PubMed
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- Levy M, Arion A, Berrebi D, et al. Severe early-onset colitis revealing mevalonate kinase deficiency. Pediatrics 2013;132:e779–83 - PubMed
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