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Article

Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination.

The Journal of investigative dermatology - 1 Mar 2018

Süßmuth Kira, Gruber Robert, Rodriguez Elke, Traupe Heiko, Amler Susanne, Sánchez-Guijo Alberto, Valentin Frederic, Tarinski Tatjana, Straub Natalia, Metze Dieter, Schneider Stefan W, Hausser Ingrid, Baurecht Hansjörg, Weidinger Stephan, Oji Vinzenz

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Identifiers

PMID: 29054605
DOI: 10.1016/j.jid.2017.08.047

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Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination.PMID 29054605Read ↗

Filaggrin haploinsufficiency among patients with dermatitis from a tertiary referral centre: early findings and possible phenotype.Semantic proximity Read ↗

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.Semantic proximity Read ↗

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic DermatitisSemantic proximity Read ↗

Ichthyosis vulgaris: the filaggrin mutation disease.Semantic proximity Read ↗

[Filaggrin gene mutations are frequent and increase the risk of skin disease].Semantic proximity Read ↗

Evidence for genetic modifiers other than filaggrin mutations in X-linked ichthyosis.Semantic proximity Read ↗

Filaggrin mutations associated with skin and allergic diseases.Semantic proximity Read ↗

X-linked and autosomal dominant forms of the ichthyosis in coinheritance.Semantic proximity Read ↗

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.Semantic proximity Read ↗

Filaggrin mutations and the skin.Semantic proximity Read ↗

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