Literature DB >> 33890311

Infliximab therapy in an infant with Netherton syndrome.

Fatih Cicek1, Sukru Cekic1, Sara Sebnem Kilic1.   

Abstract

We present a patient with Netherton syndrome and severe skin manifestations treated with infliximab. By 6 months of age, the child had intractable pruritus, scaling, dry skin, and generalized eczematous lesions resistant to conventional therapies for atopic dermatitis. Clinical improvement was observed following the third infusion of infliximab, and by 12 months of age, the skin lesions completely resolved. Infliximab is a promising option for the management of skin inflammation in Netherton syndrome, even in infants.
© 2021 Wiley Periodicals LLC.

Entities:  

Keywords:  Netherton Syndrome; childhood; ichthyosis; tumor necrosis factor-a; ınfliximab

Mesh:

Substances:

Year:  2021        PMID: 33890311     DOI: 10.1111/pde.14590

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  3 in total

1.  A novel mutation in SPINK5 gene underlies a case of atypical Netherton syndrome.

Authors:  Yu Wang; Hanqing Song; Lingling Yu; Nan Wu; Xiaodong Zheng; Bo Liang; Peiguang Wang
Journal:  Front Genet       Date:  2022-09-09       Impact factor: 4.772

2.  Cocktails of KLK5 Protease Inhibitors and Anti-TNFα Therapeutics: an Effective Treatment for Netherton Syndrome.

Authors:  Eleni Zingkou; Georgios Pampalakis; Georgia Sotiropoulou
Journal:  J Clin Immunol       Date:  2022-01-18       Impact factor: 8.317

3.  Outcomes of Systemic Treatment in Children and Adults With Netherton Syndrome: A Systematic Review.

Authors:  Anouk E M Nouwen; Renske Schappin; N Tan Nguyen; Aviël Ragamin; Anette Bygum; Christine Bodemer; Virgil A S H Dalm; Suzanne G M A Pasmans
Journal:  Front Immunol       Date:  2022-03-30       Impact factor: 8.786

  3 in total

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