| Literature DB >> 31096038 |
Reza Yazdani1, Bobak Moazzami1, Seyedeh Panid Madani1, Nasrin Behniafard2, Gholamreza Azizi3, Majid Aflatoonian4, Hassan Abolhassani5, Asghar Aghamohammadi6.
Abstract
Defects in interleukin-10 (IL10) and interleukin-10 receptors (IL10R) are closely related to very early onset (infantile) inflammatory bowel disease (VEO-IBD). In the present study, we report a novel homozygous null mutation within interleukin-10 receptor B (IL10RB) gene in a child presenting with severe VEO-IBD. In accordance with previous reports, our patient manifested with chronic diarrhea, failure to thrive, intermittent fever and multiple anal ulcers associated with Candidiasis. Homozygous null mutation within IL10RB gene (c.92C > T, p.S31P) affecting the extracellular domain of protein was discovered in this patient. In conclusion, the diagnosis of IL-10R gene mutations should always be considered as a possible cause of refractory diarrhea and failure to thrive. Mutation analysis could help detect the genetic defects associated with these clinical manifestations and to determine the most appropriate treatment option for patients affected by this disease.Entities:
Keywords: Children; Genetic defect; IL-10; Immunodeficiency; Inflammatory bowel disease; Interleukin-10 receptor
Year: 2019 PMID: 31096038 DOI: 10.1016/j.clim.2019.05.007
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969