Servicio de Información Comunitario sobre Investigación y Desarrollo - CORDIS

FP5

EUROCRAN Informe resumido

Project ID: QLG1-CT-2000-01019
Financiado con arreglo a: FP5-LIFE QUALITY
País: United Kingdom

SOX9 misregulation implicated in Pierre Robin sequence

In humans, SOX9 heterozygous mutations cause campomelic dysplasia, a syndrome with severe skeletal dysmorphology. The available evidence suggests that Sox 9 has a role in the regulation of cartilage growth and mice with the heterozygous Sox 9 mutation die perenataly with cleft palate a small lower jaw and poor formation of skeletal structure is derived from cartilage precursors. The same chromosomal breakpoint methodology identified a mutation in the region of the Sox 9 gene to be also implicated in cleft palate and a significant proportion of cleft palate patients also have mandibular hypoplasia, and this phenotype is characteristic of Pierre Robin sequence. SOX9 misregulation is therefore implicated in Pierre Robin sequence. This finding has broader implications for the pathogenesis of craniofacial deformity and also for chromatin biology and craniofacial development.

Contacto

David FITZPATRICK, (Consultant)
Tel.: +44-1316-509041
Fax: +44-1316-509031
Correo electrónico
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