📂 Diseases
autosomal dominant nonsyndromic deafness 2A — Definition
Otozomal dominant nonsendromik sağırlık 2A / autosomal dominant nonsyndromic deafness 2A
Otozomal dominant nonsendromic survival 2A is a genetic disease characterized by progressive hearing loss, usually starting in the first years or early childhood after birth. This condition is caused by structural or functional disorders in the inner ear and does not accompany other systemic symptoms (sendromic findings). The disease manifests autozomal dominant inheritance, meaning that the affected individual has a risk of seeing 50% in each child. This type, also known as DFNA2A, often starts at high frequency sounds and leads to hearing loss that affects all frequencies over time.
Frequently Asked Questions
❓ What is Otozomal dominant nonsendromik sağırlık 2A?
Otozomal dominant nonsendromik sağırlık 2A; otozomal dominant nonsendromic survival 2A is a genetic disease characterized by progressive hearing loss, usually starting in the first years or early childhood after birth. This condition is caused by structural or functional disorders in the inner ear and does not accompany other systemic symptoms (sendromic findings). The disease manifests autozomal dominant inheritance, meaning that the affected individual has a risk of seeing 50% in each child. This type, also known as DFNA2A, often starts at high frequency sounds and leads to hearing loss that affects all frequencies over time.
❓ What is autosomal dominant nonsyndromic deafness 2A in Turkish?
The Turkish equivalent of "autosomal dominant nonsyndromic deafness 2A" is Otozomal dominant nonsendromik sağırlık 2A.
❓ Which medical field is Otozomal dominant nonsendromik sağırlık 2A related to?
This term belongs to the Diseases category.