Deafness is an etiologically heterogeneous trait with many known genetic and environmental causes. Genetic factors account for at least half of all cases of profound congenital deafness, and can be classified by the mode of inheritance and the presence or absence of characteristic clinical features that may permit the diagnosis of a specific form of syndromic deafness. The identification of more than 120 independent genes for deafness has provided profound new insights into the pathophysiology of hearing, as well as many unexpected surprises. Although a large number of genes can clearly cause deafness, recessive mutations at a single locus, GJB2 or Connexin 26, account for more than half of all genetic cases in some, but not all populations.
There are three bones in the middle ear. These are the malleus, incus, and stapes. Disturbance of any of these three bones causes bone deafness.
Angleman syndrome is a genetic disorder. It can be caused by 3 or 4 difference genetic malfunctions.
conduction deafness
This is called auditory ossical fusion or fixation and it causes conductive deafness. It is usually treated by installing a hearing aide.
The most common source of genetic diversity in a bacterial colony is a mutation. External DNA is assimilated by a cell is transformation.
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.
Bruce W. Konigsmark has written: 'Genetic and metabolic deafness' -- subject(s): Deafness, Genetic aspects, Genetic aspects of Deafness, Inborn errors of Metabolism
what are the cause of partial deafness
deafness
Not at all. By MMR, I don't know if you're refering to the set of diseases (measles, mumps and rubella) or the MMR vaccine designed to immunize a person against such diseases. Either way, genetic deafness is caused by genetic factors as the name suggests. A vaccine or a virus is not going to alter your DNA to cause deafness.
Some dalmatians develop deafness as a problem.
Michael H. Fritsch has written: 'Handbook of congenital and early onset hearing loss' -- subject(s): Congenital, Deafness, Genetic aspects, Genetic aspects of Deafness, Handbooks, Hearing disorders
There are three bones in the middle ear. These are the malleus, incus, and stapes. Disturbance of any of these three bones causes bone deafness.
Temporal lobe
that would be a hereditary thing not a gene mutaion
The causes of genetic disorders areThey can be inherited through Parents;Mutations may occur;A deletion may occur.These are the causes of a genetic disorder.
Complete lack of hearing is called deafness. Various causes of deafness are defined by specific medical conditions (e.g. presbycusis - old age hearing loss). The term for less than complete deafness is "hearing impairment".