Acroniem
Stickler syndroom
Code
3F025911
Looptijd
01-10-2011 → 30-09-2015
Financiering
Regional and community funding: Special Research Fund, Research Foundation - Flanders (FWO)
Promotor
Fellow
Onderzoeksdisciplines
-
Medical and health sciences
- Laboratory medicine
- Medical systems biology
- Otorhinolaryngology
- Laboratory medicine
- Medical systems biology
- Molecular and cell biology
- Otorhinolaryngology
- Speech, language and hearing sciences
- Laboratory medicine
- Medical systems biology
- Molecular and cell biology
- Otorhinolaryngology
Trefwoorden
gehoorverlies
bindweefselziekte
genetica
stickler syndroom
schizis
Projectomschrijving
Stickler syndrome, a hereditary connective tissue disorder caused by mutations in collagen genes, has a wide variety of clinical manifestations. Currently, knowledge is lacking about otological and orofacial characteristics. In this study, we want to gain insight in this, as well as a better understanding of the molecular background and pathogenesis on hearing loss and cleft palate of Stickler syndrome.