Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia
F Almalki - Annals of Human Genetics, 2024 - Wiley Online Library
Congenital hearing loss is one of the most common sensory disabilities worldwide. The
genetic causes of hearing loss account for 50% of hearing loss. Genetic causes of hearing …
genetic causes of hearing loss account for 50% of hearing loss. Genetic causes of hearing …
A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population
Background Hearing loss is a clinically and genetically heterogeneous disorder. Mutations
in the DFNB1 locus have been reported to be the most common cause of autosomal …
in the DFNB1 locus have been reported to be the most common cause of autosomal …
Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families
The current molecular genetic diagnostic rates for hereditary hearing loss (HL) vary
considerably according to the population background. Pakistan and other countries with …
considerably according to the population background. Pakistan and other countries with …
Investigation of the genetic causes of non-syndromic hearing loss in the Western region of Saudi Arabia
K Daghistani, A Abdulkarim, A Bamanie, M Safieh… - BMC Genomics, 2014 - Springer
Background For every thousand children born in the world, there is one who is born with a
hereditary form of hearing loss. In Saudi Arabia, the rate of children affected with …
hereditary form of hearing loss. In Saudi Arabia, the rate of children affected with …
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss
Consanguineous Pakistani pedigrees segregating deafness have contributed decisively to
the discovery of 31 of the 68 genes associated with nonsyndromic autosomal recessive …
the discovery of 31 of the 68 genes associated with nonsyndromic autosomal recessive …
Epidemiology, etiology, genetic variants in non-syndromic hearing loss in Iran: A systematic review and meta‐analysis
Objectives Hearing loss is one of the most common heterogeneous complicated disorders
worldwide. We previously analyzed the results of published data on non-syndromic hearing …
worldwide. We previously analyzed the results of published data on non-syndromic hearing …
Etiology of hearing loss and genetic hearing loss
SY Kim, BY Choi - Hanyang Medical Reviews, 2015 - synapse.koreamed.org
Hearing loss is one of the most common sensory disorders and has numerous
environmental and genetic factors that influence its onset and development. Hearing loss …
environmental and genetic factors that influence its onset and development. Hearing loss …
Genetic epidemiology of hearing loss in the 22 Arab countries: a systematic review
Background: Hearing loss (HL) is a heterogeneous condition that causes partial or complete
hearing impairment. Hundreds of variants in more than 60 genes have been reported to be …
hearing impairment. Hundreds of variants in more than 60 genes have been reported to be …
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran
M Babanejad, Z Fattahi… - American journal of …, 2012 - Wiley Online Library
Hearing loss is the most common sensory disorder worldwide and affects 1 of every 500
newborns. In developed countries, at least 50% of cases are genetic, most often resulting in …
newborns. In developed countries, at least 50% of cases are genetic, most often resulting in …
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort
Background Hearing loss or hearing impairment is a clinically and genetically
heterogeneous disorder. More than 117 genes were discovered to date in hereditary …
heterogeneous disorder. More than 117 genes were discovered to date in hereditary …