Omalizumab and dupilumab for the treatment of autosomal-recessive DOCK8 hyper-IgE syndrome
Author:
Affiliation:
1. Department of Dermatology and Venereology, The first affiliated Hospital of Guangxi Medical University, Guangxi, China
Publisher
Scientific Scholar
Subject
Infectious Diseases,Dermatology
Reference4 articles.
1. Role of omalizumab in a patient with hyper-IgE syndrome and review dermatologic manifestations;Chularojanamontri;Asian Pac J Allergy Immunol,2009
2. Treatment options for DOCK8 deficiency-related severe dermatitis;Ollech;J Dermatol,2021
3. Clearance of atypical cutaneous manifestations of hyper-IgE syndrome with dupilumab;Nihal;Pediatr Dermatol,2022
4. Omalizumab for STAT3 hyper-IgE syndromes in adulthood: A case report and literature review;Lan;Front Med (Lausanne),2022
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Phenotypic and Genotypic Spectrum of Children with Autosomal Recessive Hyperimmunoglobulin E Syndrome Caused by DOCK8 Mutation: A Systematic Review of Case Reports;Indian Pediatrics Case Reports;2024-07
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