首页> 外文期刊>Psychology >Children with Down Syndrome (DS), and Autism Spectrum Disorder (ASD): Difficulties of Screening and Management of This Dual Diagnosis about 3 Cases
【24h】

Children with Down Syndrome (DS), and Autism Spectrum Disorder (ASD): Difficulties of Screening and Management of This Dual Diagnosis about 3 Cases

机译:儿童唐氏综合症(DS)和自闭症谱系障碍(ASD):这种双重诊断的筛查和管理困难约3例

获取原文
获取外文期刊封面目录资料

摘要

Down syndrome and autism spectrum disorder can be combined at the child attained; this dual diagnosis is stressful for the parents and is often overlooked by the health and education professionals of these patients. Through three observations collected at the consultation of dysmorphology of the Children’s Hospital of Rabat (CHR), this article is illustrated with the details of this association, the clarification of the data of this double diagnosis and the recommendations of good practices for the screening and early management of ASD in this population of children with special needs. The 1~(st) case: A boy, born on 02/06/2014, unique of his family, is followed for DS. The diagnosis of DS was made at birth and confirmed by the karyotype; para-clinical assessment revealed congenital hypothyroidism (CH) treated with thyroid hormones and without identification of other congenital anomalies; the 2~(nd) case: A boy, the elder of a sibling of 4, was born on 22/12/2010, the diagnosis of DS was retained from birth, the balance did not objectify congenital pathology; the 3~(rd) case: A girl was born on 03/12/2009, consanguineous relative, hypotonic, eupneic, eutrophic; a mal-formative assessment on a trisomy 47, XX, +21 karyotype was realized. Diagnosis with PEP3 and CARS shows severe autistic spectrum disorder for all three patients. In the light of these three observations and of the medical literature, the authors stress the importance of screening for precursor signs in the first year of life for early stimulation by parents and neuropsycho-educational rehabilitation, in order to ensure adequate better development of brain plasticity and thus reduce parental stress and complications related to this dual diagnosis.
机译:唐氏综合症和自闭症谱系障碍可以合并在孩子身上;这种双重诊断给父母带来了压力,并且常常被这些患者的健康和教育专业人员所忽视。通过在拉巴特儿童医院(CHR)畸形咨询会上收集到的三项观察结果,对本文进行了详细说明,并阐明了这种双重诊断的数据以及对筛查和早期筛查的良好做法的建议在这一有特殊需要的儿童人群中管理ASD。第一种情况:DS追踪了一个男孩,该男孩于2014年6月6日出生,具有他的家人的独特性。 DS的诊断是在出生时进行的,并由核型证实。辅助临床评估显示,先天性甲状腺功能减退症(CH)已用甲状腺激素治疗,未发现其他先天性异常。第二例:一个男孩,一个4岁大的兄弟姐妹,于2010年12月22日出生,从出生起就一直保留DS的诊断,其平衡并未成为先天性病理的客观表现;第三例:一名女孩,生于2009年3月12日,近亲近亲,低渗,委婉,富营养化;实现了对47,XX,+ 21三体性染色体核型的畸形评估。对PEP3和CARS的诊断显示,所有三位患者均患有严重的自闭症谱系障碍。根据这三个观察结果和医学文献,作者强调了在生命的第一年筛查先兆体征以供父母早期刺激和神经心理教育康复的重要性,以确保大脑可塑性得到适当更好的发展。从而减少与这种双重诊断有关的父母压力和并发症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号