Around 70% of genetic hearing loss are non-syndromic hearing loss. A number of gene mutations are thought to be responsible for non-syndromic hearing loss. Many of these have recently been
Around 70% of genetic hearing loss are non-syndromic hearing loss. A number of gene mutations are thought to be responsible for non-syndromic hearing loss. Many of these have recently been
Also known as (Oculo-auriculo-vertebral syndrome/dysplasia/spectrum) It is a wide spectrum of congenital anomalies that involves structure arising from first and second Branchial arches. This syndrome is characterized by incomplete development
The following are the common causes of infranuclear facial nerve paralysis: Bell’s palsy (most common) Diabetes Mellitus Post traumatic: Birth injury Temporal bone: Transverse(40-50%), Longitudinal (20%) Iatrogenic: Mastoid surgeries- most