| Literature DB >> 33538231 |
Ragaa H Salama1, Zafar Rasheed1, Ahmed A Ahmed2, Ghada A Bin Saif3, Maha M Elkholy4, Alaa E Abd El-Moniem4, Tarek Salem1, Khaled Zedan5, Ahmad A Al Robaee6, Abdullateef A Alzolibani6.
Abstract
This study investigated the atopic march on the basis of genetics. This research detected 227 variants in the filaggrin gene (FLG gene). Missense, silent, non-sense, frame-shift and non-coding mutations were detected in exon 3 of the FLG gene in patients with bronchial asthma, atopic dermatitis, allergic rhinitis and mixed atopy. Missense mutation was detected at c.8343 G > C (p. Asp2781Glu) in all adult asthmatic and allergic rhinitis patients. Whereas, mutation at c.8360 C > T/A (p. Arg2787 His/Leu) was detected in all childhood asthmatic and mixed atopic patients. A non-coding mutation was detected at c.12365 in atopic dermatitis and bronchial asthma patients. Furthermore, DNA sequencing of asthmatic and mixed atopic patients showed missense mutations at c.6073 C > T (p. Gly2025Glu) and a silent mutation at c. 8341 G > A (p. Asp2781Asp).Entities:
Keywords: Mutations; allergic rhinitis; asthma; atopic dermatitis; atopic march; filaggrin
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Year: 2021 PMID: 33538231 DOI: 10.1080/15257770.2021.1880009
Source DB: PubMed Journal: Nucleosides Nucleotides Nucleic Acids ISSN: 1525-7770 Impact factor: 1.381