📂 Diseases
autosomal dominant nonsyndromic deafness 3A — Definition
Otozomal dominant nonsendromik sağırlık 3A / autosomal dominant nonsyndromic deafness 3A
Otozomal dominant nonsendromic survival 3A is a genetic hearing disorder, characterized by high frequency hearing loss, usually starting from 10-30 years. The disease is caused by mutations in WFS1 gene and affects only hearing function without other systemic findings. Hearing loss can cover all frequencies by transmitting over time and may vary strength. This situation indicates the paterni of autozomal dominant inheritance, meaning the risk of seeing the disease in every child affected by the affected individual is 50%.
Frequently Asked Questions
❓ What is Otozomal dominant nonsendromik sağırlık 3A?
Otozomal dominant nonsendromik sağırlık 3A; otozomal dominant nonsendromic survival 3A is a genetic hearing disorder, characterized by high frequency hearing loss, usually starting from 10-30 years. The disease is caused by mutations in WFS1 gene and affects only hearing function without other systemic findings. Hearing loss can cover all frequencies by transmitting over time and may vary strength. This situation indicates the paterni of autozomal dominant inheritance, meaning the risk of seeing the disease in every child affected by the affected individual is 50%.
❓ What is autosomal dominant nonsyndromic deafness 3A in Turkish?
The Turkish equivalent of "autosomal dominant nonsyndromic deafness 3A" is Otozomal dominant nonsendromik sağırlık 3A.
❓ Which medical field is Otozomal dominant nonsendromik sağırlık 3A related to?
This term belongs to the Diseases category.