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Aetiologic spectrum of mental retardation & developmental delay in India.

机译:印度精神发育迟滞的病因学谱。

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Background & objectives: The aetiology of mental retardation is varied and difficult to establish. Reports from India on the spectrum of underlying causative conditions are lacking. This retrospective study was conducted to establish the various aetiologies of mental retardation (MR) and developmental delay (DD) in patients attending a medical genetics centre in north India and to assess the contribution of genetic disorders. Methods: This retrospective study was conducted at a tertiary care centre in north India. All patients attending the centre with MR or DD from January 2007 to December 2009 were included. The aetiology of MR/DD was ascertained after clinical assessment and targeted laboratory evaluation. The spectrum of causative conditions and contribution of genetic disorders was established. Results: A total of 338 patients were included in the study, of whom definite diagnosis was established in 253 (74.8%). The various aetiological categories were: chromosomal disorders in 112 (33.1%), non chromosomal syndromes in 32 (9.5%), neurometabolic disorders in 34 (10.1%), central nervous system structural defects in 25 (7.4%), cerebral palsy in 43 (12.7%) and environmental insults in 7 (2%). Eighty five patients (25.2%) had idiopathic mental retardation. A total of 196 (58%) patients had a genetic disorder as the cause of MR/DD. Interpretation & conclusions: The aetiology of MR/DD is varied and difficult to establish in a significant proportion of patients. Chromosomal and various monogenic disorders contribute to a large number of MR/DD cases and hence a genetic work up is essential for all such patients.
机译:背景与目的:智力低下的病因多种多样且难以确立。缺乏印度有关潜在病因范围的报告。进行了这项回顾性研究,目的是确定印度北部医学遗传学中心就诊患者的智力低下(MR)和发育迟缓(DD)的各种病因,并评估遗传疾病的影响。方法:这项回顾性研究在印度北部的一家三级医疗中心进行。纳入了2007年1月至2009年12月在中心接受MR或DD治疗的所有患者。经过临床评估和有针对性的实验室评估后,确定了MR / DD的病因。确定了致病条件和遗传疾病贡献的范围。结果:共纳入338例患者,其中253例确诊(74.8%)。各种病因分类为:染色体疾病112例(33.1%),非染色体综合征32例(9.5%),神经代谢异常34例(10.1%),中枢神经系统结构缺陷25例(7.4%),脑性瘫痪43例(12.7%)和环境侮辱7(2%)。八十五名患者(25.2%)患有特发性智力低下。共有196名(58%)患者患有遗传性疾病,成为MR / DD的病因。解释与结论:MR / DD的病因多种多样,并且在很大比例的患者中难以确定。染色体和各种单基因疾病会导致大量MR / DD病例,因此对所有此类患者进行基因检查是必不可少的。

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