Genetic Deafness
Inner ear (sensori-neural hearing loss)
Research Models and Biological Samples
Clinical Resources
Therapeutic and Diagnostic Development
Syndromic hearing loss with temporal bones malformation
Patient Cohorts
5 patient cohort (pediatric)
Isolated hearing loss
Patient Cohorts
50 pediatric patient with LHFPL5 mutations – 30 pediatric patient with OTOF mutations – Patients with GJB2 mutations (please contact us)
Patient Cohorts
Patient cohort
Syndromic hearing loss without temporal bones malformation
Patient Cohorts
10 patient cohort (pediatric)
Syndromic Usher syndrome 1
Patient Cohorts
> 100 patient cohort (pediatric)
Syndromic Usher syndrome 2
Patient Cohorts
> 100 patient cohort (pediatric)
Syndromic Usher syndrome 3
Patient Cohorts
> 100 patient cohort (pediatric)
With auditory nerve malformations
Patient Cohorts
5 patients (pediatric)
With auditory nerve malformations (unknown genetic cause)
Patient Cohorts
50 pediatric patients
Isolated auditory neuropathy
Syndromic auditory neuropathy
Syndromic Heimler syndrome
Patient Cohorts
10 patient cohort (pediatric)
