| Literature DB >> 32951242 |
Meryem Aktas1, Andac Salman1, Ozlem Apti Sengun1, Elif Comert Ozer1, Selcen Hosgoren Tekin1, Ozlem Akin Cakici1, Gizem Demir1, Tulin Ergun1.
Abstract
Netherton syndrome (NS) is an orphan disease characterized by congenital ichthyosis, hair abnormalities, and atopy, with limited treatment options. We achieved temporary improvement only during the initial 6 weeks of treatment with dupilumab, which differs from the sustained improvement observed in 2 other recently published cases. Although the clinical presentation of atopy and increased pre-allergic cytokines in NS patients suggest that dupilumab may be beneficial, larger studies are required.Entities:
Keywords: Ichthyosis; atopic eczema; genetic diseases/mechanisms
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Year: 2020 PMID: 32951242 DOI: 10.1111/pde.14362
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588