نتایج جستجو برای: autosomal recessive non syndromic hearing loss

تعداد نتایج: 1782138  

Journal: :iranian journal of basic medical sciences 0
masoumeh falah department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran massoud houshmand national institute for genetic engineering and biotechnology, tehran, iran susan akbaroghli tehran welfare organization, tehran, iran saeid mahmodian department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran yaser ghavami department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran mohammad farhadi department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran

objective(s) despite the enormous heterogeneity of genetic hearing loss, most non-syndromic hearing losses are caused by mutations in the gjb2 gene. we aimed to characterize the mutation profiles of 100 iranian deaf patients that were under 10 years old. materials and methods patients were tested with direct sequencing of entire coding region of the gjb2 gene. results eight known mutations plus...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2013
Bushra Afroze Bushra Chaudhry

Non-syndromic mental retardation is one of the most serious neurodevelopmental disorders, which has a serious impact not only on the affected individuals and their families but also on the health care system and society. Previously research has been more focused on the X-linked mental retardation and only recently studies have shown that non-syndromic autosomal recessive mental retardation is e...

2018
Farah Talebi Farideh Ghanbari Mardasi Javad Mohammadi Asl Saeed Tizno Marziye Najafvand Zadeh

Autosomal recessive non-syndromic hearing loss (ARNSHL) is defined as a genetically heterogeneous disorder. The aim of the present study was to screen for pathogenic variants in an Iranian pedigree with ARNSHL. Next-generation targeted sequencing of 127 deafness genes in the proband detected two novel variants, a homozygous missense variant in PTPRQ (c.2599 T>C, p.Ser867Pro and a heterozygous m...

Journal: :Journal of medical genetics 1992
L Jaber M Shohat X Bu N Fischel-Ghodsian H Y Yang S J Wang J I Rotter

We present here a large Israeli-Arab kindred with hereditary deafness. In this family 55 deaf subjects (29M, 26F), who are otherwise healthy, have been identified and traced back five generations to one common female ancestor. The deafness is progressive in nature, usually presenting in infancy and childhood. Audiometry on six deaf and seven unaffected subjects was consistent with severe to pro...

Journal: :Journal of medical genetics 2002
S H Blanton C Y Liang M W Cai A Pandya L L Du B Landa S Mummalanni K S Li Z Y Chen X N Qin Y F Liu T Balkany W E Nance X Z Liu

We have studied 36 subjects in a large multigenerational Chinese family that is segregating for an autosomal dominant adult onset form of progressive non-syndromic hearing loss. All affected subjects had bilateral sensorineural hearing loss involving all frequencies with some significant gender differences in initial presentation. After excluding linkage to known loci for non-syndromic deafness...

Journal: :European journal of medical genetics 2014
Érika L Freitas Jeanne Oiticica Amanda G Silva Roseli S M Bittar Carla Rosenberg Regina C Mingroni-Netto

In 20% of cases, hereditary non-syndromic hearing loss has an autosomal dominant inheritance (ADNSHL). To date, more than 50 loci for ADNSHL have been mapped to different chromosomal regions. In order to verify whether genomic alterations contribute to the hearing loss etiology and to search for novel deafness candidate loci, we investigated probands from families with ADNSHL by oligonucleotide...

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