نتایج جستجو برای: deafness autosomal recessive 59

تعداد نتایج: 115286  

Journal: :international journal of molecular and cellular medicine 0
saeid morovvati research center for human genetics, baqiyatallah university of medical sciences, mollasadra st, tehran (postal box: 19395-5487), iran sara amirpour amaraii tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran hosna zahed shekarabi tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran nastaran shahbazi tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran

in the rare hereditary bone disorder of osteopetrosis, reduced bone resorption function leads to both the development of densely sclerotic fragile bones and progressive obliteration of the marrow spaces and cranial foramina. marrow obliteration, typically associated with extramedullary hemopoiesis and hepatosplenomegaly, results in anemia and thrombocytopenia and nerve entrapment accounts for p...

Journal: :Bulletin de la Societe belge d'ophtalmologie 2001
K Van den Abeele M Craen J Schuil F M Meire

The Alström syndrome is a rare autosomal recessive disorder characterized by pigmentary retinopathy, diabetes mellitus, sensorineural deafness and obesity. A normal intelligence is often present. We report 9 patients.

Journal: :Archives of otolaryngology--head & neck surgery 2001
A H Chen D A Stephan T Hasson K Fukushima C M Nelissen A F Chen A I Jun A Ramesh G Van Camp R J Smith

BACKGROUND Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2 and 19p13.3-13.1, identifying one of these chromosomal regions (or possibly both) as the site of a deafness-causing gene. Mutations in unconventional myosins cause deafness in mice and humans. One unconventional myosin, myosin 1F (MYO1F), is expressed in the cochlea an...

Journal: :International Journal of Pediatric Otorhinolaryngology 2021

Hereditary non-syndromic hearing loss (NSHL) has a high genetic heterogeneity with about 152 genes identified as associated molecular causes. The present study aimed to detect the possible damaging variants of deaf probands from six unrelated Chinese families. After excluding pathogenic/likely pathogenic in most common genes, GJB2 and SLC26A4, 12 prelingual deafness autosomal recessive inherita...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
اعظم السادات هاشمی a hashemi . [email protected] عبدالحمید جعفری ah jafari مریم خیراندیش m kheirandish خدیجه دهقانی kh dehghani فروغ السادات نورانی f nourani فاطمه متوسلیان f motavaselian

thiamine responsive megaloblastic anemia in didmoa (wolfram) syndrome has an autosomal- recessive mode of inheritance . megaloblastic anemia and sideroblastic anemia is accompanied by diabetes insipidus (di), diabetes mellitus (dm) ,optic atrophy (oa) and deafness (d). neutropenia and thrombocytopenia are also present. we report a 7 month old girl with congenital macrocytic anemia a rare clinic...

2015
Malika Dahmani Fatima Ammar-Khodja Crystel Bonnet Gaelle M. Lefèvre Jean-Pierre Hardelin Hassina Ibrahim Zahia Mallek Christine Petit

BACKGROUND More than 70 % of the cases of congenital deafness are of genetic origin, of which approximately 80 % are non-syndromic and show autosomal recessive transmission (DFNB forms). To date, 60 DFNB genes have been identified, most of which cause congenital, severe to profound deafness, whereas a few cause delayed progressive deafness in childhood. We report the study of two Algerian sibli...

2014
Yu Su Wen-Xue Tang Xue Gao Fei Yu Zhi-Yao Dai Jian-Dong Zhao Yu Lu Fei Ji Sha-Sha Huang Yong-Yi Yuan Ming-Yu Han Yue-Shuai Song Yu-Hua Zhu Dong-Yang Kang Dong-Yi HAN Pu Dai

TECTA-related deafness can be inherited as autosomal-dominant nonsyndromic deafness (designated DFNA) or as the autosomal-recessive version. The α-tectorin protein, which is encoded by the TECTA gene, is one of the major components of the tectorial membrane in the inner ear. Using targeted DNA capture and massively parallel sequencing (MPS), we screened 42 genes known to be responsible for huma...

2017
Amnah Y Bdier Saleh Al-Ghamdi Prashant K Verma Khalid Dagriri Bandar Alshehri Omamah A Jiman Sherif E Ahmed Arthur A M Wilde Zahurul A Bhuiyan Jumana Y Al-Aama

BACKGROUND One of the most common primary cardiac arrhythmia syndromes is autosomal dominant long QT syndrome, type 1 (LQT1), chiefly caused by mono-allelic mutations in the KCNQ1 gene. Bi-allelic mutations in the KCNQ1 gene are causal to Jervell and Lange-Nielsen syndrome (JLNS), characterized by severe and early-onset arrhythmias with prolonged QTc interval on surface ECG and sensorineural de...

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