نتایج جستجو برای: x gene mutations

تعداد نتایج: 1789763  

Background and aims: Hearing loss (HL) happens due to the genetic or environmental causes or both. Risk factors include congenital infections and congenital deformities of auricle and ear duct. The present study was performed to briefly explain the genetics, molecular biology and epidemiology of HL in Middle East especially in Iran. Methods: An intense an...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
منصور صالحی m salehi . [email protected] رسول صالحی r salehi بهرام نصر اصفهانی b nasr- esfahani

introduction: mucopolysaccharidosis i (mps-i) is an autosomal recessive lysosomal storage diseases, caused by α-l-iduronidase (idua) enzyme deficiency. the clinical manifestations of mps-i patients are variable ranging from severe to mild, and therefore prediction of disease severity is difficult. from when idua gene has been cloned more than 109 distinct mutations have been identified in it an...

ژورنال: پژوهش در پزشکی 2012
ابراهیمی دریانی, ناصر, بالایی, هدیه, حبیبی, منیژه, زالی, محمد رضا, زجاجی, همایون, شریفیان, افسانه, فرنود, آلما, نادری, نصرت اله,

Abstract Background: NOD2 gene located on chromosome 16 (IBD1) is known to have a strong association with Crohn’s disease. Three common polymorphisms of this gene including R702W, G908R, 1007fsinsC, were reported to be frequent in many western populations while rare occurrence of them was observed in eastern countries. The aim of this study was to assess the frequency of these polymorphisms ...

ژورنال: پژوهش در پزشکی 2005

Background : Most of the offending genes of diseases are quite big and complex with varieties of exons. Gene montage is a new technique for formation of a big linked DNA segment that could be easily detected by DNA sequencing or Denaturing High Performance Liquid Chromatography (DHPLC). Methods : Exons 2,20,23 and 24 of BRCA1 gene were linked and analyzed by DNA sequencing. Exons 2 and 20 are i...

ابهجی, مریم, اسمیت, ریچارد, بزاز زادگان, نیلوفر, جوان, محمد خلیل, خدایی, حسین, دهقانی, عاطفه, ریاض الحسینی, یاسر, سیفتی, مرتضی, مغنی باشی, مهدی, میراب, محمود, نجم آبادی, حسین, کهریزی, کیمیا,

Introduction: Hearing loss is the most common sensory neural defect in humans, affecting 1 in 1000 neonates, with over half of these cases predicted to be hereditary in nature. Most hereditary hearing loss is inherited in a recessive fashion, accounting for approximately 80 % of non-syndromic hearing loss (NSHL). Mutations in GJB2 gene are major cause of inherited deafness in the European an...

ژورنال: Hormozgan Medical Journal 2011
Abolhasani, M, Asghari, A, Azadeghan, F, Banitalebi Dehkordi, G, Farrokhi, E, Hashemzadeh Chaleshtori, M, Hoseinipor, A, Keshavarz, S, Montazer Zohori, M, Saeedi Morghmaleki, M,

Introduction: Hearing loss is the most frequent sensory disorder occurs in 1/1000 newborns. About 50% of hearing loss cases are due to genetic causes. Mutation in MTRNR1(A1555G), MTTL1(A3243G) and MTTS1(A7445G) are known to be one of the important cause of nonsyndromic Sensorineural hearing loos in some populations. This study aims to demonstrate the frequency of three mitochondrial mutatio...

Journal: :international journal of pediatrics 0
soudeh ghafouri-fard department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. shadab salehpour department of pediatrics, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. vahidreza yassaee genomic research center, shahid beheshti university of medical sciences, tehran, iran. mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, iran.

background the x-linked cyclin-dependent kinase like 5 (cdkl5/stk9) gene has been shown to be responsible for a severe encephalopathy condition characterized by early onset of epilepsy and severe developmental delay. cdkl5 mutations have been shown to be more frequent among female patients. results here we report a 6- month male patient, second child of a healthy non consanguineous in the irani...

Arezou Karamzade, Elaheh Alavinejad, Hassan Khojasteh Jafari, Mohammad Keramatipour, Mohammad Saberi, Mona Entezam, Yeganeh Eshaghkhani, Zahra Golchehre,

Background: Leber congenital amaurosis (LCA) is a rare inherited retinal disease causing severe visual impairment in infancy. It has been reported that 9-15% of LCA cases have mutations in CRB1 gene. The complex of CRB1 protein with other associated proteins affects the determination of cell polarity, orientation, and morphogenesis of photoreceptors. Here, we report three novel pathogenic varia...

Journal: :Journal of child neurology 2004
Jong Hee Chae Hee Hwang Yong Seung Hwang Hee Jung Cheong Ki Joong Kim

To date, approximately 200 different mutations in the MECP2 gene have been identified. We analyzed the entire coding sequence of the MECP2 gene and the X-chromosome inactivation pattern in 42 sporadic cases of Rett syndrome. Of the 42 patients, 30 had pathogenic mutations, including 14 different mutations: 9 missense mutations, 4 nonsense mutations, and 1 frameshift mutation. One was a novel mu...

Abolfazl Akbari, Fariba Ghassemi Ghasem Fakhraie, Mansour Heidari, Masoumeh Mohebi, Mehran Zarei-Ghanavati Nahid Babaie Saeed Chenari,

Objective(s): Childhood cataract is a genetically heterogeneous eye disorder that results in visual impairment. The aim of this study was to identify the genetic mutations of connexin 50 gene among Iranian families suffered from autosomal dominant congenital cataracts (ADCC). Materials and Methods: Families, having at least two members with bilateral familial congenital cataract, were selected ...

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