نتایج جستجو برای: syndromic autosomal recessive hearing loss

تعداد نتایج: 526049  

Journal: :Clinical genetics 2012
G Borck L Rainshtein S Hellman-Aharony A E Volk K Friedrich E Taub N Magal M Kanaan C Kubisch M Shohat L Basel-Vanagaite

Autosomal-recessive non-syndromic hearing impairment (DFNB) is usually of prelingual onset with a moderate to profound degree of hearing loss. More than 70 DFNB loci have been mapped and ~40 causative genes have been identified. Non-syndromic hearing impairment caused by mutations of DFNB59 (encoding pejvakin) has been described in a couple of families in which affected individuals presented wi...

آهنگری, نجمه, مسعودی, مرجان, نجاتی زاده, عبدالعظیم, پورصادق, علی اکبر,

Background & Objective: Deafness is the most common sensory disorder in humans which is highly heterogeneous. Among its various types, autosomal recessive non-syndromic hearing loss (ARNSHL) is responsible for 80% of pre-speech congenital cases of hearing loss. The purpose of this study was to investigate the genetic linkage of DFNB4 locus in hearing impaired families in Hormozgan. Method: Te...

2016
Somayeh Reiisi Mohammad Amin Tabatabaiefar Mohammad Hosein Sanati Morteza Hashemzadeh Chaleshtori

OBJECTIVES Non-syndromic sensorineural hearing loss (NSHL) is a common disorder affecting approximately 1 in 500 newborns. This type of hearing loss is extremely heterogeneous and includes over 100 loci. Mutations in the GJB2 gene have been implicated in about half of autosomal recessive non-syndromic hearing loss (ARNSHL) cases, making this the most common cause of ARNSHL. For the latter form ...

Journal: :Human molecular genetics 2003
Zubair M Ahmed Saima Riazuddin Jamil Ahmad Steve L Bernstein Yan Guo Muhammad F Sabar Paul Sieving Sheikh Riazuddin Andrew J Griffith Thomas B Friedman Inna A Belyantseva Edward R Wilcox

Recessive splice site and nonsense mutations of PCDH15, encoding protocadherin 15, are known to cause deafness and retinitis pigmentosa in Usher syndrome type 1F (USH1F). Here we report that non-syndromic recessive hearing loss (DFNB23) is caused by missense mutations of PCDH15. This suggests a genotype-phenotype correlation in which hypomorphic alleles cause non-syndromic hearing loss, while m...

Journal: :Human molecular genetics 1996
A Veske R Oehlmann F Younus A Mohyuddin B Müller-Myhsok S Q Mehdi A Gal

Autosomal recessive childhood-onset non-syndromic deafness is one of the most frequent forms of inherited hearing impairment. Recently five different chromosomal regions, 7q31, 11q13.5, 13q12, 14q and the pericentromeric region of chromosome 17, have been shown to harbour disease loci for this type of neurosensory deafness. We have studied a large family from Pakistan, containing several consan...

Journal: :Human molecular genetics 1999
P J Coucke P Van Hauwe P M Kelley H Kunst I Schatteman D Van Velzen J Meyers R J Ensink M Verstreken F Declau H Marres K Kastury S Bhasin W T McGuirt R J Smith C W Cremers P Van de Heyning P J Willems S D Smith G Van Camp

We have previously found linkage to chromosome 1p34 in five large families with autosomal dominant non-syndromic hearing impairment (DFNA2). In all five families, the connexin31 gene ( GJB3 ), located at 1p34 and responsible for non-syndromic autosomal dominant hearing loss in two small Chinese families, has been excluded as the responsible gene. Recently, a fourth member of the KCNQ branch of ...

Journal: :iranian journal of public health 0
m hashemzadeh chaleshtori dd farhud ma patton

background: mutations in the gjb2 gene encoding connexin 26 protein, are the main cause for autosomal recessive and sporadic non syndromic hearing loss in many populations. here, we have taken together and reviewed results from our six previous publications, our unpublished data from ten iranian provinces, as well as data from two previous mutation reports to provide a comprehensive collection ...

Journal: :iranian journal of public health 0
m hashemzadeh chaleshtori l hoghooghi rad m dolati r sasanfar a hoseinipour m montazer zohour

while hearing loss has been considered to be a very heterogeneous disorder, mutations in gap junction beta 2 (gjb2) gene encoding connexin 26 (cx26) protein are the major cause of autosomal recessive and sporadic non-syndromic deafness in many populations. in this study, we have investigated the prevalence of the gjb2 gene mutations using nested pcr pre screening strategy and direct sequencing ...

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