نتایج جستجو برای: deafness autosomal recessive 59

تعداد نتایج: 115286  

Journal: :iranian journal of basic medical sciences 0
seyyedha abbas foundation university medical college (fumc), islamabad, pakistan abdul khaliq naveed army medical college, national university of sciences &technology.rawalpindi, pakistan shakir khan margalla medical and dental college, islamabad, pakistan muhammad jawad yousaf army medical college, national university of sciences & technology, rawalpindi, pakistan zahid azeem ajk medical college, muzaffrahbad, ajk, pakistan suhail razak biochemistry and molecular biology,army medical college, national university of sciences & technology, rawalpindi, pakistan

objective(s): genetic analysis of two consanguineous pakistani families with localized autosomal recessive hypotrichosis was performed with the goal to establish genotype-phenotype correlation. materials and methods: genomic dna extraction had been done from peripheral blood samples. extracted dna was then subjected to pcr (polymerase chain reaction) for amplification. linkage analysis was perf...

Journal: :Genetic testing and molecular biomarkers 2009
Mortaza Bonyadi Mohsen Esmaeili Masoumeh Abhari Alireza Lotfi

AIMS Mutations in the GJB2 gene-encoding connexin 26 protein are the main cause for autosomal recessive nonsyndromic hearing loss worldwide. In this study, we assessed the contributions made by GJB2 and del(GJB6-D13S1830) mutations to the autosomal recessive nonsyndromic deafness genetic load in Iranian Azeri Turkish patients. RESULTS Probands from 209 different nuclear families were investig...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2007
Martin Schwander Anna Sczaniecka Nicolas Grillet Janice S Bailey Matthew Avenarius Hossein Najmabadi Brian M Steffy Glenn C Federe Erica A Lagler Raheleh Banan Rudy Hice Laura Grabowski-Boase Elisabeth M Keithley Allen F Ryan Gary D Housley Tim Wiltshire Richard J H Smith Lisa M Tarantino Ulrich Müller

Deafness is the most common form of sensory impairment in the human population and is frequently caused by recessive mutations. To obtain animal models for recessive forms of deafness and to identify genes that control the development and function of the auditory sense organs, we performed a forward genetics screen in mice. We identified 13 mouse lines with defects in auditory function and six ...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
محمد رضا مرتضوی زاده mr mortazavizadeh . [email protected] فریبا بینش f binesh امیر بهرامی احمدی a bahrami- ahmadi

thiamine responsive megaloblastic anemia (trma), also known as roger syndrome is an autosomal recessive disorder resulting from the deficiency of thiamine (vitamin b1) transporter protein. this is the report of a 3- year follow up of a female child who presented in 2000 at the age of 11 with severe anemia, congenital deafness and diabetes mellitus. in our follow-up period we prescribed 100-mg t...

Journal: :Archives of otolaryngology--head & neck surgery 2001
S Marlin E N Garabédian G Roger L Moatti N Matha P Lewin C Petit F Denoyelle

OBJECTIVE To evaluate difficulties encountered in genetic counseling in deaf children carrying connexin 26 gene (CX26 or GJB2) mutations. DESIGN Prospective study. SETTING Outpatients, tertiary referral center. PATIENTS Ninety-six unrelated deaf children in whom CX26 mutations had been detected consecutively. Children were recruited to a center for genetic counseling for deaf children, an...

2009
Masyita Gaffar Freddy G. Kuhuwael Irawan Yusuf

Background: Inherited hearing impairment affects about 1 in 1000 newborns. Up to 50 percent of all patients with autosomal recessive nonsyndromic prelingual deafness in many populations have mutations in the gene encoding the gap junction protein connexin 26 (GJB2) at locus DFNB1 (autosomal recessive nonsyndromic deafness) on chromosome 13q11-12. In East Asia, there is a common mutation (235del...

Journal: :Pediatric dentistry 1989
W K Seow

In this study, a possible new syndrome affecting 18 members of a family spanning 4 generations is described. The main features include palmoplantar hyperkeratosis, proportionate short stature, facial dysmorphism, clinodactyly, epilepsy, deafness, and hypodontia. This syndrome is inherited in an autosomal dominant manner with a high degree of penetrance but variable expressivity. This syndrome d...

Journal: :Human molecular genetics 2012
Sedigheh Delmaghani Asadollah Aghaie Nicolas Michalski Crystel Bonnet Dominique Weil Christine Petit

We report a consanguineous Iranian family affected by congenital profound sensorineural deafness segregating in an autosomal recessive mode. Auditory tests implicated at least a cochlear defect in these patients. We mapped the deafness, autosomal recessive (DFNB) locus involved by linkage analysis to a 4.8 Mb region at chromosome 21q22.3-qter. Exclusion of the DFNB8/10 gene TMPRSS3, located in ...

2016
So Young Kim Ah Reum Kim Nayoung K. D. Kim Chung Lee Min Young Kim Eun-Hee Jeon Woong-Yang Park Byung Yoon Choi

The molecular etiology of nonsyndromic sensorineural hearing loss (SNHL) in subjects with only one detectable autosomal recessive GJB2 mutation is unclear. Here, we report GJB2 single heterozygotes with various final genetic diagnoses and suggest appropriate diagnostic strategies. A total of 160 subjects with SNHL without phenotypic markers were screened for GJB2 mutations. Single-nucleotide va...

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