📂 Diseases
autosomal recessive nonsyndromic deafness 3 — Definition
Otozomal resesif nonsendromik sağırlık 3 / autosomal recessive nonsyndromic deafness 3
Otozomal resesif nonsendromic survival 3 is a genetic disease, usually manifested innate or early childhood, causing hearing loss. This condition only affects hearing function without other systemic findings and indicates autozomal resesif inheritance. The disease is usually caused by structural or functional disorders in the inner ear, and is characterized by irradiating, moderate to very advanced sensorine hearing loss. It is confirmed by diagnosis, clinical evaluation and genetic tests.
Frequently Asked Questions
❓ What is Otozomal resesif nonsendromik sağırlık 3?
Otozomal resesif nonsendromik sağırlık 3; otozomal resesif nonsendromic survival 3 is a genetic disease, usually manifested innate or early childhood, causing hearing loss. This condition only affects hearing function without other systemic findings and indicates autozomal resesif inheritance. The disease is usually caused by structural or functional disorders in the inner ear, and is characterized by irradiating, moderate to very advanced sensorine hearing loss. It is confirmed by diagnosis, clinical evaluation and genetic tests.
❓ What is autosomal recessive nonsyndromic deafness 3 in Turkish?
The Turkish equivalent of "autosomal recessive nonsyndromic deafness 3" is Otozomal resesif nonsendromik sağırlık 3.
❓ Which medical field is Otozomal resesif nonsendromik sağırlık 3 related to?
This term belongs to the Diseases category.