Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum

Autor(es):Mostrar menos -

Cavalcanti, Denise P. ^{[1, 2]} ; Huber, Celine ^[1] ; Sang, Kim-Hanh Le Quan ^[1] ; Baujat, Genevieve ^[1] ; Collins, Felicity ^[3] ; Delezoide, Anne-Lise ^[4] ; Dagoneau, Nathalie ^[1] ; Le Merrer, Martine ^[1] ; Martinovic, Jelena ^[5] ; Mello, Marcos Fernando S. ^[6] ; Vekemans, Michel ^[1] ; Munnich, Arnold ^[1] ; Cormier-Daire, Valerie ^[1]

Afiliação do(s) autor(es)

^[1] Univ Paris 05, Dept Genet, INSERM, Hop Necker Enfants Malad, AP HP, U781, Paris - France

^[2] Univ Estadual Campinas, Programa Genet Perinatal, Dept Med Genet, FCM, BR-13081970 Campinas, SP - Brazil

^[3] Childrens Hosp Westmead, Western Sydney Genet Program, Dept Clin Genet, Sydney, NSW - Australia

^[4] Univ Paris Diderot, Serv Biol Dev, Hop Robert Debre, Paris - France

^[5] Hop Necker Enfants Malad, Unit Fetal Pathol, Dept Histoembryol & Cytogenet, Paris - France

^[6] Univ Estadual Campinas, Dept Pathol, FCM, BR-13081970 Campinas, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: JOURNAL OF MEDICAL GENETICS; v. 48, n. 2, p. 88-92, FEB 2011.
• Citações Web of Science: 38

Resumo

Background The lethal group of short-rib polydactyly (SRP) includes type I (Saldino-Noonan; MIM 263530), type II (Majewski; MIM 263520), type III (Verma-Naumoff; MIM 263510) and type IV (Beemer-Langer; MIM 269860). Jeune and Ellis-van Creveld dysplasias also used to be classified in the SRP group. Recently, mutations in a gene encoding a protein involved in intraflagellar transport, IFT80, have been identified in 3/39 patients with Jeune dysplasia but no extraskeletal manifestation. Methods Because of clinical and radiological similarities between Jeune dysplasia and the other lethal types of SRP, the authors decided to investigate IFT80 in a cohort of fetuses with the lethal forms of SRP (Majewski, Verma-Naumoff and Beemer-Langer) and antenatally diagnosed cases of Jeune dysplasia. Fifteen fetuses were identified. A double-molecular approach was adopted. For consanguineous families and for those with recurrent sibs, a haplotype analysis around the gene locus was first performed, and, for the others, all the coding exons of IFT80 were directly sequenced. Results Using the haplotype approach for two families, the authors excluded the IFT80 region as a candidate for them. Direct sequencing of IFT80 in the other 13 cases showed a G-to-C transversion in exon 8 (G241R) in only one SRP case closely related to the type III phenotype. Conclusions The findings show that mutations in IFT80 can also be responsible for a lethal form of SRP and provide the molecular basis for the Jeune-Verma-Naumoff dysplasia spectrum. (AU)

• Processo FAPESP: 98/16006-6 - Estudo da etiopatogenia dos defeitos congênitos de alta morbi-mortalidade no período perinatal
• Beneficiário: Denise Pontes Cavalcanti
• Modalidade de apoio: Auxílio à Pesquisa - Regular