نتایج جستجو برای: autosomal recessive non syndromic hearing loss

تعداد نتایج: 1782138  

2004
R Li J H Greinwald

H earing loss is a very common congenital disorder affecting one in 1000 newborns. More than 50% of deafness cases in the paediatric population have a genetic cause with autosomal dominant, autosomal recessive, X-linked, or mitochondrial patterns of inheritance. Mutations in mitochondrial DNA (mtDNA), particularly in the 12S rRNA and tRNA genes, have been found to be one of the most important c...

Journal: :International journal of clinical and experimental pathology 2012
Nobutaka Ohgami Haruka Tamura Kyoko Ohgami Machiko Iida Ichiro Yajima Mayuko Y Kumasaka Yuji Goto Michihiko Sone Tsutomu Nakashima Masashi Kato

About 120 million people worldwide suffer from congenital (early-onset) hearing loss. Thirty percent of them have syndromic hearing loss and the remaining 70% have non-syndromic hearing loss. In addition, a large number of elderly people worldwide suffer from age-related (late-onset) hearing loss. c-Ret and c-RET have been shown to be essential for the development and maintenance of neurons inc...

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...

2007
Suzan R. Ismail Mervat M. Hashishe Mona I. Mourad Manal Abdel-Kader

The study comprised 25 patients with Syndromic genetic hearing loss. They were selected from the Audiology Unit, Faculty of Medicine, and the Human Genetics clinic, Medical Research Institute, , Alexandria University. Their ages ranged from 2.5 to 19 years. Males were more affected than females (M/F ratio = 2:1). T he high parental consanguinity (63.2 %) emphasizes the contribution of autosomal...

2017
Abdelaziz Tlili Abdullah Fahd Al Mutery Mona Mahfood Walaa Kamal Eddine Ahmad Mohamed Khalid Bajou

Autosomal recessive non-syndromic hearing loss is one of the most common monogenic diseases. It is characterized by high allelic and locus heterogeneities that make a precise diagnosis difficult. In this study, whole-exome sequencing was performed for an affected patient allowing us to identify a new frameshift mutation (c.804delG) in the Immunoglobulin-Like Domain containing Receptor-1 (ILDR1)...

Journal: :Medical Journal Armed Forces India 2015

Journal: :Bioinformatics 2006
Quan-Yuan He Xiang-Hua Liu Qiang Li David J. Studholme Xuan-Wen Li Song-Ping Liang

UNLABELLED We report a novel protein domain-G8-which contains five repeated beta-strand pairs and is present in some disease-related proteins such as PKHD1, KIAA1199, TMEM2 as well as other uncharacterized proteins. Most G8-containing proteins are predicted to be membrane-integral or secreted. The G8 domain may be involved in extracellular ligand binding and catalysis. It has been reported that...

2012
Kerry A. Miller Louise H. Williams Elizabeth Rose Michael Kuiper Hans-Henrik M. Dahl Shehnaaz S. M. Manji

Human MYO7A mutations can cause a variety of conditions involving the inner ear. These include dominant and recessive non-syndromic hearing loss and syndromic conditions such as Usher syndrome. Mouse models of deafness allow us to investigate functional pathways involved in normal and abnormal hearing processes. We present two novel mouse models with mutations in the Myo7a gene with distinct ph...

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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