Congenital deafness
Congenital deafness refers to deafness that has existed since birth. It can be divided into hereditary and non-hereditary; it is mainly autosomal recessive, accounting for more than 75%, non-hereditary congenital deafness accounts for about 20%, hereditary deafness is divided into non-syndromic and syndrome (syndromic) two categories, accounting for about 80% and 20%, respectively. There is also a type of deafness caused by mitochondrial disease. Non-hereditary deafness can be caused by congenital infection, metabolic factors in pregnant women, and so on.
The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.