A novel candidate gene in autosomal dominant facial pruritus.

Thompson, B A; Dear, K; Donaldson, E; Nixon, R; Winship, I M

Thompson, B A; Dear, K; Donaldson, E; Nixon, R; Winship, I M.

Affiliation

Thompson BA; Department of Pathology, Royal Melbourne Hospital, Parkville, Vic., Australia.
Dear K; Department of Genomic Medicine, Royal Melbourne Hospital, Parkville, Vic, Australia.
Donaldson E; Occupational Dermatology Research and Education Centre, Skin Health Institute, Carlton, Vic., Australia.
Nixon R; Department of Genomic Medicine, Royal Melbourne Hospital, Parkville, Vic, Australia.
Winship IM; Occupational Dermatology Research and Education Centre, Skin Health Institute, Carlton, Vic., Australia.

Clin Exp Dermatol ; 47(1): 184-186, 2022 Jan.

Article de En | MEDLINE | ID: mdl-34386996

ABSTRACT

ABSTRACT

In the clinical investigation of a family with debilitating centrofacial pruritus by exome sequencing, we have observed a clear segregation of the TRPM3 variant outlined, which is highly suggestive of a causal relationship.

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Prurit / Canaux cationiques TRPM / Dermatoses faciales Limites: Female / Humans / Middle aged Langue: En Journal: Clin Exp Dermatol Année: 2022 Type de document: Article Pays d'affiliation: Australie

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