Add to ORKGAbstract Autosomal-recessive genes account for about 80% of the patients of non-syndromic deafness, and a major portion of those lead to cochlear pathology. Given the strong cultural practice of consanguineous marriages and the lack of awareness regarding screening modalities, a high prevalence of hereditary pre-lingual deafness is seen in Pakistan. Considering the situation, cochlear implant surgery was introduced by Aga Khan University Hospital (AKUH), Karachi, Pakistan, in 2003. Recently we decided to expand the profile and services available and conducted the first ever cochlear implant on an anatomically-challenged cochlea. The case report relates to the experience of our pilot patient who was suffering from Mondini\u27s deformity
Abstract The magnitude of hearing loss in Pakistan is enormous. One in twelve children of Pakistan s...
Goldenhar Syndrome is a rare syndrome which affects most of the characteristic features of that part...
A 4-month-old baby girl whose parents and 6-year-old brother have severe-to-profound sensorineural h...
Abstract Autosomal-recessive genes account for about 80% of the patients of non-syndromic deafness, ...
We report the speech perception progress and programming procedures of a case of congenital profound...
Hearing impairment is a significant disability. According to the World Health Organization (WHO), mo...
Hearing loss is one of the world’s leading causes of chronic health conditions. Cochlea plays a vita...
Background: Although cochlear implantation has been almost a standard otological procedure worldwide...
Many children have benefited from cochlear implant device including those with congenital malformati...
Abstract Introduction: Estimates of the magnitude of consanguinity related profound bilateral senso...
Cochlear implantation has become established worldwide as a safe and effective method of auditory re...
Objectives: To determine the prevalence of inner ear anomalies and the frequency of different anomal...
Objectives: The Chudley-McCullough Syndrome (CMS) is a rare autosomal-recessively inherited disorder...
Introduction: Literature regarding the different degrees of hearing loss in patients with Cornelia d...
Introduction. Cochlear implantation (CI) was a significant surgical innovation in the 20th century a...
Abstract The magnitude of hearing loss in Pakistan is enormous. One in twelve children of Pakistan s...
Goldenhar Syndrome is a rare syndrome which affects most of the characteristic features of that part...
A 4-month-old baby girl whose parents and 6-year-old brother have severe-to-profound sensorineural h...
Abstract Autosomal-recessive genes account for about 80% of the patients of non-syndromic deafness, ...
We report the speech perception progress and programming procedures of a case of congenital profound...
Hearing impairment is a significant disability. According to the World Health Organization (WHO), mo...
Hearing loss is one of the world’s leading causes of chronic health conditions. Cochlea plays a vita...
Background: Although cochlear implantation has been almost a standard otological procedure worldwide...
Many children have benefited from cochlear implant device including those with congenital malformati...
Abstract Introduction: Estimates of the magnitude of consanguinity related profound bilateral senso...
Cochlear implantation has become established worldwide as a safe and effective method of auditory re...
Objectives: To determine the prevalence of inner ear anomalies and the frequency of different anomal...
Objectives: The Chudley-McCullough Syndrome (CMS) is a rare autosomal-recessively inherited disorder...
Introduction: Literature regarding the different degrees of hearing loss in patients with Cornelia d...
Introduction. Cochlear implantation (CI) was a significant surgical innovation in the 20th century a...
Abstract The magnitude of hearing loss in Pakistan is enormous. One in twelve children of Pakistan s...
Goldenhar Syndrome is a rare syndrome which affects most of the characteristic features of that part...
A 4-month-old baby girl whose parents and 6-year-old brother have severe-to-profound sensorineural h...