突变SYNGAP-1和Catatonia:一个案例系列和系统审查
Isaac Baldwin1, Alicia Cho2, Gabe Orenstein2
1Division of Child and Adolescent Psychiatry, Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Journal of child and adolescent psychopharmacology
|September 5, 2024
概括
在患有SYNGAP-1突变和自闭症谱系障碍 (ASD) 的儿童中,过度活跃的catatonia经常被遗漏. 在这些患者中识别白症症状对于有效治疗和改善生活质量至关重要.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 过度活跃的猫头在儿科患者群体中经常被诊断不足,特别是在那些患有神经发育障碍的人群中,如自闭症谱系障碍 (ASD).
- 新兴研究表明,过度活跃的猫头在自伤和ASD中的侵略中起着重要作用,需要进一步调查.
- 已知SYNGAP-1基因突变是发育障碍的已知原因,其与catatonia的关联需要探索.
结论:
- 显著的症状重叠表明,在SYNGAP-1突变的个体中,catatonia的诊断可能不足.
- 自伤行为和攻击性,常见于多动性猫症,是SYNGAP-1相关疾病的关键特征.
- 临床医生应考虑在SYNGAP-1突变患者的这些症状的差异诊断中考虑catatonia,因为及时治疗可以提高安全性和福祉.
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