摩洛哥智力残疾临床特征研究。

Q3 Medicine
Innovations in clinical neuroscience Pub Date : 2024-09-01 eCollection Date: 2024-07-01
Houda Bekkari, Yousra Benmakhlouf, Naima Ghailani Nourouti, Amina Barakat, Mohcine Bennani Mechita
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引用次数: 0

摘要

目的:智障(Intellectual Disability,ID)被认为是人类最常见的疾病之一,其特点是在认知、功能和适应能力方面存在严重缺陷。本研究旨在描述生活在丹吉尔-特图安地区的一组摩洛哥智障人士的人口统计学和临床特征:这是一项回顾性和描述性的探索性单中心研究,研究时间为 2020 年 11 月至 2023 年 8 月。共纳入 109 名智障患者。这些患者均来自丹吉尔-特图安地区的四家精神健康中心。我们使用 IBM SPSS 26 版本对数据进行了处理和分析:在我们的系列研究中发现,ID 患者中男性居多(男性占 54.4%,女性占 42.6%)。男女比例为 1.34。患者的平均年龄为(11.75±4.87)岁,标准差(SD)为 1 至 35 岁。智障子女出生时,母亲和父亲的平均年龄分别为 28.36 岁和 35.6 岁。在我们的数据中发现了许多并发症(语言发育迟缓:20.5%;注意力不集中:15.1%;多动:11.1%;行走困难:8.8%;攻击性:8.8%):8.8%、攻击性:8%、视力问题:6.3%、癫痫发作:4%):4%).近亲结婚率为 26.9%:结论:在摩洛哥人口中,与遗传原因相关的智障与近亲结婚率密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of Clinical Characteristics of Intellectual Disability in Morocco.

Objective: Intellectual disability (ID) is considered one of the most common human disorders characterized by significant deficits in cognition and functional and adaptive skills. The aims of this study were to describe the demographic and clinical features of a group of Moroccan individuals with ID living in the Tangier-Tetouan region.

Design: This was a retro-prospective and descriptive exploratory monocentric study realized between November 2020 and August 2023. A total of 109 patients with ID were included. They were selected at four mental health centers in the Tangier-Tetouan region. Our data were treated and analyzed using the IBM SPSS version 26.

Results: A male predominance of patients with ID was observed in our series (54.4% male vs. 42.6% female). The male-to-female ratio was 1.34. The mean±standard deviation (SD) age of our patients was 11.75±4.87 years, ranging from 1 to 35 years. The mean ages of mothers and fathers at the births of their children with ID were 28.36 and 35.6 years, respectively. Many co-occurring medical conditions were noted in our data (speech delay: 20.5%, concentration problems: 15.1%, hyperactivity: 11.1%, ambulation difficulties: 8.8%, aggressiveness: 8%, vision problems: 6.3%, epileptic seizures: 4%). The consanguinity rate was 26.9 percent.

Conclusion: ID associated with genetic causes was significantly correlated with the consanguinity rate in the Moroccan population.

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来源期刊
Innovations in clinical neuroscience
Innovations in clinical neuroscience Medicine-Psychiatry and Mental Health
CiteScore
2.10
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0.00%
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