منابع مشابه
Genetic Causes of Putative Autosomal Recessive Intellectual Disability Cases in Hamedan Province
Objective: The aim of this study was to investigate the genetic causes of autosomal recessive intellectual disabilities (AR-ID) in Hamadan province of Iran. Materials & Methods: In this descriptive-analytical cross-sectional study, 25 families with more than one affected with putative autosomal recessive intellectual disability were chosen with collaboration of Welfare Organization of Hamada...
متن کاملNational disability registers report on causes of intellectual disability in Taiwan: 2000-2007.
The main purposes of the present analysis were to describe the causes of intellectual disability (ID) and examine its overtime change from 2000 to 2007 in Taiwan. Data of the present study mainly come from the public web-access information which collected by the Department of Statistics, Ministry of the Interiors, Taipei, Taiwan. Data were obtained from two ways of 2000-2007 national data: (1) ...
متن کاملDiagnostic approach for genetic causes of intellectual disability
Received: 1 December 2014, Revised: 28 February 2015, Accepted: 28 February 2015, Published: 30 June 2015 *Corresponding author: Shin-Young Yim, M.D., Ph.D. The Children’s Rehabilitation Clinic, Department of Physical Medicine and Rehabilitation, Department of Medical Genetics, Ajou University School of Medicine, 164 Worldcup-ro, Yeongtong-gu, Suwon 443-380, Korea. Tel: +82-31-219-5284, Fax: +8...
متن کاملCauses of visual disability among Central Africans with diabetes mellitus.
BACKGROUND Diabetic Retinopathy (DR) remains a common and one of the major causes of blindness in the developed and western societies. The same situation is shown in emerging economic areas (5,6). In sub-Saharan Africa (SSA) however, the issues of visual disability due to diabetes mellitus (DM) are overshadowed by the presence of the prevalent and common nutritional deficiency diseases and eye ...
متن کاملBCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Intellectual disability (ID) is a common condition with considerable genetic heterogeneity. Next-generation sequencing of large cohorts has identified an increasing number of genes implicated in ID, but their roles in neurodevelopment remain largely unexplored. Here we report an ID syndrome caused by de novo heterozygous missense, nonsense, and frameshift mutations in BCL11A, encoding a transcr...
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ژورنال
عنوان ژورنال: Southern Medical Journal
سال: 1910
ISSN: 0038-4348
DOI: 10.1097/00007611-191003000-00028