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Case Reports
. 2020 Jul;183(1):165-167.
doi: 10.1111/bjd.18892. Epub 2020 Mar 9.

Successful treatment of Netherton syndrome with ustekinumab in a 15-year-old girl

S Volc  1 , L Maier  2   3 , A Gritsch  2 , M C Aichelburg  2 , B Volc-Platzer  2   3
Affiliations
Case Reports

Successful treatment of Netherton syndrome with ustekinumab in a 15-year-old girl

S Volc et al. Br J Dermatol. 2020 Jul.
No abstract available

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References

    1. Renner ED, Hartl D, Rylaarsdam S et al. Comèl-Netherton syndrome defined as primary immunodeficiency. J Allergy Clin Immunol 2009; 124:536-43.
    1. Mazereeuw-Hautier J, Vahlquist A, Traupe H et al. Management of congenital ichthyoses: European Guidelines of care, part one. Br J Dermatol 2019; 180:272-81.
    1. Paller AS, Renert-Yuval Y, Suprun M et al. An IL-17-dominant immune profile is shared across the major orphan forms of ichthyosis. J Allergy Clin Immunol 2017; 139:152-65.
    1. Fontao L, Laffitte E, Briot A et al. Infliximab infusions for Netherton syndrome: sustained clinical improvement correlates with a reduction of thymic stromal lymphopoietin levels in the skin. J Invest Dermatol 2011; 131:1947-50.
    1. Lwin SM, Hsu CK, Liu L et al. Beneficial effect of ustekinumab in familial pityriasis rubra pilaris with a new missense mutation in CARD14. Br J Dermatol 2018; 178:969-72.