📂 Diseases
autosomal dominant nonsyndromic deafness 3B — Definition
Otozomal dominant nonsendromik sağırlık 3B / autosomal dominant nonsyndromic deafness 3B
Otozomal dominant nonsendromic survival 3B is a genetic disease that causes hearing loss but does not accompany other systemic or physical findings. The disease manifests autozomal dominant inheritance, meaning that the affected individual is likely to inherit disease in every child. It is often characterized by a progressive hearing loss that occurs after childbirth or early childhood. This situation is caused by structural or functional disorders in the inner ear and usually starts with difficulty in the detection of high frequency sounds.
Frequently Asked Questions
❓ What is Otozomal dominant nonsendromik sağırlık 3B?
Otozomal dominant nonsendromik sağırlık 3B; otozomal dominant nonsendromic survival 3B is a genetic disease that causes hearing loss but does not accompany other systemic or physical findings. The disease manifests autozomal dominant inheritance, meaning that the affected individual is likely to inherit disease in every child. It is often characterized by a progressive hearing loss that occurs after childbirth or early childhood. This situation is caused by structural or functional disorders in the inner ear and usually starts with difficulty in the detection of high frequency sounds.
❓ What is autosomal dominant nonsyndromic deafness 3B in Turkish?
The Turkish equivalent of "autosomal dominant nonsyndromic deafness 3B" is Otozomal dominant nonsendromik sağırlık 3B.
❓ Which medical field is Otozomal dominant nonsendromik sağırlık 3B related to?
This term belongs to the Diseases category.