نتایج جستجو برای: autosomal recessive nonsyndromic hearing loss arnshl

تعداد نتایج: 522522  

Journal: :American journal of human genetics 2005
Rikkert L Snoeckx Patrick L M Huygen Delphine Feldmann Sandrine Marlin Françoise Denoyelle Jaroslaw Waligora Malgorzata Mueller-Malesinska Agneszka Pollak Rafal Ploski Alessandra Murgia Eva Orzan Pierangela Castorina Umberto Ambrosetti Ewa Nowakowska-Szyrwinska Jerzy Bal Wojciech Wiszniewski Andreas R Janecke Doris Nekahm-Heis Pavel Seeman Olga Bendova Margaret A Kenna Anna Frangulov Heidi L Rehm Mustafa Tekin Armagan Incesulu Hans-Henrik M Dahl Desirée du Sart Lucy Jenkins Deirdre Lucas Maria Bitner-Glindzicz Karen B Avraham Zippora Brownstein Ignacio del Castillo Felipe Moreno Nikolaus Blin Markus Pfister Istvan Sziklai Timea Toth Philip M Kelley Edward S Cohn Lionel Van Maldergem Pascale Hilbert Anne-Françoise Roux Michel Mondain Lies H Hoefsloot Cor W R J Cremers Tuija Löppönen Heikki Löppönen Agnete Parving Karen Gronskov Iris Schrijver Joseph Roberson Francesca Gualandi Alessandro Martini Geneviéve Lina-Granade Nathalie Pallares-Ruiz Céu Correia Graça Fialho Kim Cryns Nele Hilgert Paul Van de Heyning Carla J Nishimura Richard J H Smith Guy Van Camp

Hearing impairment (HI) affects 1 in 650 newborns, which makes it the most common congenital sensory impairment. Despite extraordinary genetic heterogeneity, mutations in one gene, GJB2, which encodes the connexin 26 protein and is involved in inner ear homeostasis, are found in up to 50% of patients with autosomal recessive nonsyndromic hearing loss. Because of the high frequency of GJB2 mutat...

2011
Masoud Motasaddi Zarandy Mersedeh Rohanizadegan Hojjat Salmasian Nooshin Nikzad Niloofar Bazazzadegan Mahdi Malekpour

Clinical application of mutation screening and its effect on the outcome of cochlear implantation is widely debated. We investigated the effect of mutations in GJB2 gene on the outcome of cochlear implantation in a population with a high rate of consanguineous marriage and autosomal recessive nonsyndromic hearing loss. Two hundred and one children with profound prelingual sensorineural hearing ...

Journal: :Human mutation 2006
Juan R González Wenyi Wang Ester Ballana Xavier Estivill

Mutations in the DFNB1 locus, where two connexin genes are located (GJB2 and GJB6), account for half of congenital cases of nonsyndromic autosomal recessive deafness. Because of the high frequency of DFNB1 gene mutations and the availability of genetic diagnostic tests involving these genes, they are the best candidates to develop a risk prediction model of being hearing impaired. People underg...

Journal: :ORL; journal for oto-rhino-laryngology and its related specialties 2006
Yildirim A Bayazit Metin Yilmaz

Understanding the genetic basis of hearing loss is important because almost 50% of profound hearing loss are caused by genetic factors and more than 120 independent genes have been identified. In this review, after a brief explanation of some genetic terms (allele, heterozygosis, homozygosis, polymorphism, genotype and phenotype), classification of genetic hearing loss (syndromic versus nonsynd...

Journal: :Gene 1998
D A Scott J H Greinwald J R Marietta S Drury R E Swiderski A Viñas M M DeAngelis R Carmi A Ramesh M L Kraft K Elbedour A B Skworak R A Friedman C R Srikumari Srisailapathy K Verhoeven G Van Gamp M Lovett P L Deininger M A Batzer C C Morton B J Keats R J Smith V C Sheffield

The DFNB7/11 locus for autosomal recessive non-syndromic hearing loss (ARNSHL) has been mapped to an approx. 1.5 Mb interval on human chromosome 9q13-q21. We have determined the cDNA sequence and genomic structure of a novel cochlear-expressed gene, ZNF216, that maps to the DFNB7/11 interval. The mouse orthologue of this gene maps to the murine dn (deafness) locus on mouse chromosome 19. The ZN...

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