Autosomal Hearing Loss

The condition in which trained is hearing loss or inability to hear right from birth is referred to as congenital hearing loss. Genetic factors play an important role in related cases. Also the factors coeval prenatally ( in utero ) could be guilty for hearing loss from birth.

Autosomal hearing loss is essentially related to chromosomes ( any delete the sex chromosome ) and the identical can be best explained as below - Autosomal hearing loss may be Autosomal controlling hearing loss - In this case, one author carries the controlling gene for hearing loss and typically has a hearing loss passes it on to the child. In uniform a case, trained is at first off a 50 % chance that the child will also have a hearing loss. The chances are higher if both the parents have the governing gene ( where both parents have a hearing loss also ). This can smooth happen if both grandparents on one side of the family have hearing loss due to genetic causes.

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Autosomal commanding hearing loss is expected if the child is detected with Treacher Collins syndrome as it is a confessed sequence of this syndrome.

Autosomal recessive hearing loss - In this rundown, generally both the parents have average hearing but one or both may be carrying a recessive gene. In such a situation, the child usually has a 25 % chance of hearing loss as everybody else in the family has normal hearing. Autosomal recessive hearing loss is expected if the child is detected with Usher syndrome as it is a known effect of this particular syndrome.

Autosomal hearing loss once diagnosed and evaluated, can be managed by using an appropriate habilitation option. Use of hearing aids, vibrotactile devices and cochlear implantation are some of the possible treatment options.

An experienced team consisting of an otolaryngologist, an audiologist, a clinical geneticist and a pediatrician should be able to help with treatment for autosomal hearing loss.

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