📂 Diseases
autosomal recessive nonsyndromic deafness 61 — Definition
Otozomal resesif nonsendromik sağırlık 61 / autosomal recessive nonsyndromic deafness 61
Otozomal resesif nonsendromic vigilance 61 is a genetic disease where hearing loss can be seen alone, accompanied by other systemic findings. This condition, also known as DFNB61, is characterized by non-compressive or slow forward sensor hearing loss, usually manifested innate or early childhood. The disease manifests autozomal resesif inheritance, meaning it is seen in individuals who have a copy of mutational gene from both parents.
Frequently Asked Questions
❓ What is Otozomal resesif nonsendromik sağırlık 61?
Otozomal resesif nonsendromik sağırlık 61; otozomal resesif nonsendromic vigilance 61 is a genetic disease where hearing loss can be seen alone, accompanied by other systemic findings. This condition, also known as DFNB61, is characterized by non-compressive or slow forward sensor hearing loss, usually manifested innate or early childhood. The disease manifests autozomal resesif inheritance, meaning it is seen in individuals who have a copy of mutational gene from both parents.
❓ What is autosomal recessive nonsyndromic deafness 61 in Turkish?
The Turkish equivalent of "autosomal recessive nonsyndromic deafness 61" is Otozomal resesif nonsendromik sağırlık 61.
❓ Which medical field is Otozomal resesif nonsendromik sağırlık 61 related to?
This term belongs to the Diseases category.