نتایج جستجو برای: deafness autosomal recessive 59

تعداد نتایج: 115286  

2009
H. Bouzidi M. Daudon M. F. Najjar Tahar Sfar

Renal tubular acidosis are forms of metabolic acidosis characterized by an impairment of urinary acidification due to a lack of urine excretion of protons or loss of bicarbonates. Primary distal renal acidosis (dRTA) is characterized by hyperchloremic metabolic acidosis due to failure in proton excretion, variably severe nephrocalcinosis and/or nephrolithiasis associated with hypercalciuria and...

تیموری, حسین, مجتبوی نائینی, مرجان, معتمدی, سمیرا, هاشم زاده چالشتری, مرتضی,

Background and Objective: TMC1 gene mutations are known as the most common causes of autosomal recessive non-syndromic hearing loss (ARNSHL) in different populations. According to large size of the TMC1 gene and the large number of identified mutations in this gene, application of polymorphic markers is suggested for carrier detection and prenatal diagnosis in families. In this study, informati...

Journal: :American journal of medical genetics. Part A 2011
Niloofar Bazazzadegan Abraham M Sheffield Masoomeh Sobhani Kimia Kahrizi Nicole C Meyer Guy Van Camp Nele Hilgert Seyedeh Sedigheh Abedini Farkhondeh Habibi Ahmad Daneshi Carla Nishimura Matthew R Avenarius Mohammad Farhadi Richard J H Smith Hossein Najmabadi

Mutations in GJB2, encoding connexin 26 (Cx26), cause both autosomal dominant and autosomal recessive nonsyndromic hearing loss (ARNSHL) at the DFNA3 and DFNB1 loci, respectively. Most of the over 100 described GJB2 mutations cause ARNSHL. Only a minority has been associated with autosomal dominant hearing loss. In this study, we present two families with autosomal dominant nonsyndromic hearing...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012
Katja Strasser Julia Hoefele Carsten Bergmann Anja K Büscher Rainer Büscher Peter F Hoyer Stefanie Weber

Alport syndrome (ATS) is a type-IV collagen inherited disorder, caused by mutations in COL4A3 and COL4A4 (autosomal recessive) or COL4A5 (X-linked). Clinical symptoms include progressive renal disease, eye abnormalities and high-tone sensorineural deafness. A renal histology very similar to ATS is observed in a subset of patients affected by mutations in MYH9, encoding non-muscle-myosin Type II...

Objective(s): Jervell and Lange–Nielsen syndrome is an autosomal recessive disorder caused by mutations in KCNQ1 or KCNE1 genes. The disease is characterized by sensorineural hearing loss and long QT syndrome. Methods: Here we present a 3.5-year-old female patient, an offspring of consanguineous marriage, who had a history of recurrent syncope and congenital sensorineural deafness. The patient ...

Journal: :Human molecular genetics 1997
F Denoyelle D Weil M A Maw S A Wilcox N J Lench D R Allen-Powell A H Osborn H H Dahl A Middleton M J Houseman C Dodé S Marlin A Boulila-ElGaïed M Grati H Ayadi S BenArab P Bitoun G Lina-Granade J Godet M Mustapha J Loiselet E El-Zir A Aubois A Joannard J Levilliers E N Garabédian R F Mueller R J Gardner C Petit

Prelingual non-syndromic (isolated) deafness is the most frequent hereditary sensory defect. In >80% of the cases, the mode of transmission is autosomal recessive. To date, 14 loci have been identified for the recessive forms (DFNB loci). For two of them, DFNB1 and DFNB2, the genes responsible have been characterized; they encode connexin 26 and myosin VIIA, respectively. In order to evaluate t...

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