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