📂 الأمراض
autosomal recessive nonsyndromic deafness 101 — التعريف
Otozomal resesif nonsendromik sağırlık 101 / autosomal recessive nonsyndromic deafness 101
Otozomal resesif nonsendromic survival 101 is a genetic disease caused by hearing loss and does not accompany other systemic findings. The disease manifests autozomal resesif inheritance, meaning it is necessary to transfer mutational gene from both parents. It is characterized by bilateral and advanced sensor hearing loss, usually manifested in birth or early child. This condition is caused by mutations in TMC1 gene and leads to dysfunction of the function of hair cells in the inner ear.
الأسئلة الشائعة
❓ ما هو Otozomal resesif nonsendromik sağırlık 101؟
Otozomal resesif nonsendromik sağırlık 101; otozomal resesif nonsendromic survival 101 is a genetic disease caused by hearing loss and does not accompany other systemic findings. The disease manifests autozomal resesif inheritance, meaning it is necessary to transfer mutational gene from both parents. It is characterized by bilateral and advanced sensor hearing loss, usually manifested in birth or early child. This condition is caused by mutations in TMC1 gene and leads to dysfunction of the function of hair cells in the inner ear.
❓ ما معنى autosomal recessive nonsyndromic deafness 101 بالتركية؟
المعادل التركي لـ "autosomal recessive nonsyndromic deafness 101" هو Otozomal resesif nonsendromik sağırlık 101.
❓ ما هو المجال الطبي الذي يتعلق بـ Otozomal resesif nonsendromik sağırlık 101؟
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