Congenital ichthyosiform erythroderma due to a CYP4F22 mutation responds to ustekinumab: A case report and review of the literature
J Eur Acad Dermatol Venereol
.
2023 Mar;37(3):e389-e391.
doi: 10.1111/jdv.18605.
Epub 2022 Oct 7.
Authors
Myriam Viedma-Martínez
1
,
David Jiménez-Gallo
1
,
Irene Navarro-Navarro
1
,
José Francisco Millán-Cayetano
1
,
Mario Linares-Barrios
1
Affiliation
1
Unidad de Gestión Clínica de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario Puerta del Mar, Cádiz, Spain.
PMID:
36165166
DOI:
10.1111/jdv.18605
No abstract available
Publication types
Review
Case Reports
Letter
MeSH terms
Humans
Ichthyosiform Erythroderma, Congenital* / drug therapy
Ichthyosiform Erythroderma, Congenital* / genetics
Mutation
Ustekinumab* / therapeutic use
Substances
Ustekinumab