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Condition: Eczema

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Total 2491 results found since Jan 2013.

Phenotype of Atopic Dermatitis With Food Allergy Predicts Development of Childhood Asthma via Gut Wnt Signaling
CONCLUSIONS: When FA is present in various phenotypes of AD at early life, regardless of severity of eczema, it may be associated with gut Wnt signaling and later development of asthma.PMID:36426397 | PMC:PMC9709687 | DOI:10.4168/aair.2022.14.6.674
Source: Allergy, Asthma and Immunology Research - November 25, 2022 Category: Allergy & Immunology Authors: So-Yeon Lee Sangrok Kim Mi Jin Kang Kun-Baek Song Eom Ji Choi Sungsu Jung Ji-Sun Yoon Dong In Suh Youn Ho Shin Kyung Won Kim Kangmo Ahn Soo-Jong Hong Source Type: research

Prevalence and Influencing Factors of Food Allergy in Global Context: A Meta-Analysis
Conclusion: There were geographical differences in the prevalence of FA. Identification and nursing of FA high-risk populations should be strengthened to improve the quality of life.Int Arch Allergy Immunol
Source: International Archives of Allergy and Immunology - January 12, 2023 Category: Allergy & Immunology Source Type: research

Phenotype of Atopic Dermatitis With Food Allergy Predicts Development of Childhood Asthma via Gut Wnt Signaling
CONCLUSIONS: When FA is present in various phenotypes of AD at early life, regardless of severity of eczema, it may be associated with gut Wnt signaling and later development of asthma.PMID:36426397 | PMC:PMC9709687 | DOI:10.4168/aair.2022.14.6.674
Source: Allergy, Asthma and Immunology Research - November 25, 2022 Category: Allergy & Immunology Authors: So-Yeon Lee Sangrok Kim Mi Jin Kang Kun-Baek Song Eom Ji Choi Sungsu Jung Ji-Sun Yoon Dong In Suh Youn Ho Shin Kyung Won Kim Kangmo Ahn Soo-Jong Hong Source Type: research

Detection of Six Novel Mutations in WASP Gene in Fifteen Iranian Wiskott-Aldrich Patients.
Abstract Wiskott-Aldrich syndrome (WAS) is a life-threatening X-linked recessive immunodeficiency disease described as a clinical triad of thrombocytopenia, eczema, and recurrent infections, caused by mutations of the WAS protein (WASP) gene. The milder form of this disease is X-Linked thrombocytopenia (XLT) that presents only as platelet abnormalities. Mutation analysis for 15 boys with Wiskott-Aldrich syndrome was performed. Five previously reported mutations and six novel mutations including G8X, R41X, D283E, P412fsX446, E464X, and AfsX358 were detected. PMID: 23264413 [PubMed - in process]
Source: Iranian Journal of Allergy, Asthma and Immunology - December 1, 2012 Category: Allergy & Immunology Authors: Safaei S, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Alavi S, Mousavi F, Pourpak Z, Moin M Tags: Iran J Allergy Asthma Immunol Source Type: research