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The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.
Blaydon, Diana C; Ishii, Yoshiyuki; O'Toole, Edel A; Unsworth, Harriet C; Teh, Muy-Teck; Rüschendorf, Franz; Sinclair, Claire; Hopsu-Havu, Väinö K; Tidman, Nicholas; Moss, Celia; Watson, Rosemarie; de Berker, David; Wajid, Muhammad; Christiano, Angela M; Kelsell, David P.
Afiliación
  • Blaydon DC; Centre for Cutaneous Research, Institute of Cell & Molecular Science, Queen Mary's School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, London E1 4AT, UK.
Nat Genet ; 38(11): 1245-7, 2006 Nov.
Article en En | MEDLINE | ID: mdl-17041604
Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which the only presenting phenotype is the absence or severe hypoplasia of all fingernails and toenails. After determining linkage to chromosome 20p13, we identified homozygous or compound heterozygous mutations in the gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, in eight affected families. Rspo4 expression was specifically localized to developing mouse nail mesenchyme at embryonic day 15.5, suggesting a crucial role in nail morphogenesis.
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Bases de datos: MEDLINE Asunto principal: Trombospondinas / Proteínas Wnt / Uñas Malformadas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2006 Tipo del documento: Article
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Bases de datos: MEDLINE Asunto principal: Trombospondinas / Proteínas Wnt / Uñas Malformadas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2006 Tipo del documento: Article