Tiwari Shivani, Kallianpur Divya, DeSilva Kelly Ann
Department of Speech and Hearing, School of Allied Health Sciences, Manipal University, Manipal, Karnataka, India.
Indian J Psychol Med. 2017 Mar-Apr;39(2):146-151. doi: 10.4103/0253-7176.203125.
Inborn Errors of Metabolism (IEMs) are a group of complex genetic conditions, predominantly affecting the pediatric population. While the understanding and identification of various IEMs has significantly improved over recent times, not much is known about the communication disorders in this population. The present study focused on identification and profiling of communication impairments in children diagnosed with IEMs.
Data was obtained retrospectively from medical records of children visiting a tertiary care hospital over a period of ten years (2005 - 2014). Selected data was reviewed to obtain demographic details, clinical signs/manifestations, laboratory findings, risk factors, developmental disorders and reported communication impairments.
The findings of the study showed a variety of clinical signs and laboratory findings in children with inborn errors of metabolism. A few of the risk factors observed in the group were consanguinity, sibling death and family history of other disorders. Many children with IEM displayed communication disorders, most common as the delay in speech and language development.
The results of this study showed that various communication disorders were seen in almost half of the children with a diagnosis of IEM. Findings are discussed with implications for future research in this direction.
先天性代谢缺陷(IEMs)是一组复杂的遗传疾病,主要影响儿童群体。虽然近年来对各种IEMs的认识和识别有了显著提高,但对该群体中的沟通障碍了解不多。本研究聚焦于诊断为IEMs的儿童沟通障碍的识别和特征分析。
回顾性收集一家三级护理医院十年(2005 - 2014年)期间就诊儿童的病历资料。对所选数据进行审查,以获取人口统计学细节、临床体征/表现、实验室检查结果、风险因素、发育障碍及报告的沟通障碍情况。
研究结果显示,先天性代谢缺陷儿童存在多种临床体征和实验室检查结果。该组中观察到的一些风险因素包括近亲结婚、兄弟姐妹死亡及其他疾病家族史。许多IEM患儿存在沟通障碍,最常见的是言语和语言发育迟缓。
本研究结果表明,近一半诊断为IEM的儿童存在各种沟通障碍。讨论了这些发现对该方向未来研究的启示。