Conditions / Genetic
otosclerosis 11
info ยท Genetic
An otosclerosis that is characterized by onset of progressive hearing loss in the second to third decade of life and that has_material_basis_in the locus associated with Forkhead Box L1 gene (FOXL1) on chromosome 16q24.
Signs and symptoms
- Conductive hearing impairment
- Absence of acoustic reflex
- Otosclerosis
- Sensorineural hearing impairment
Also known as: OTSC11