Hereditary deafness is typically diagnosed through a combination of medical history, physical examinations, and audiological evaluations. Genetic testing may also be conducted to identify specific mutations associated with hearing loss. Newborn hearing screenings and follow-up assessments in children can help detect deafness early, while adults may undergo comprehensive hearing tests to assess the extent and type of hearing loss. Consulting with an audiologist or genetic counselor can provide further insights into hereditary patterns and potential interventions.
c. cochlea
help pls His problem involves the Cochlea! Tha answer is Cochlea
This is because genes are inherited and herditary is a scientific way of saying inherited, used when talking about inherited diseases and genes. Hope this helps! :)
DNA but they have no nucleus. They are Prokaryotes.
Post- Vocational Deafness:
what are the cause of partial deafness
Deafness is when somone is unable to hear anything.
Like allergies and birthmarks, deafness as a symptom by itself is not genetic. Deafness as a symptom of a disease which is genetic, is genetic.
Anacusis is the medical term meaning complete deafness.
Inborn Deafness is a trouble speaking or general fusion
deafness, trouble speaking, general confusion
His despair was deafness