Conditions / Genetic

X-linked deafness 3

info ยท Genetic

An X-linked nonsyndromic deafness characterized by congenital, bilateral, profound and sensorineural hearing loss in males and bilateral, mild to moderate high frequency sensorineural hearing impairment with later onset in heterozygous females that has_materia

An X-linked nonsyndromic deafness characterized by congenital, bilateral, profound and sensorineural hearing loss in males and bilateral, mild to moderate high frequency sensorineural hearing impairment with later onset in heterozygous females that has_material_basis_in mutation in a region on chromosome Xp21.2.

Signs and symptoms

  • Congenital sensorineural hearing impairment

Also known as: DFN4; DFNX3; congenital sensorineural X-linked deafness 4