跨年龄组的 Chung-Jansen 综合征患者的临床表型
Khemika K Sudnawa1,2, Sean Calamia1, Alexa Geltzeiler1
1Department of Pediatrics, Columbia University, New York, New York, USA.
American journal of medical genetics. Part A
|November 14, 2023
概括
Pleckstrin 同源域相互作用蛋白 (PHIP) 中的致病变体会导致 Chung-Jansen 综合征. 这项研究详细介绍了47个人的表型和基因型,强调了常见的症状和早期干预的必要性.
科学领域:
- 遗传学 遗传学 是一个
- 神经发育障碍 神经发育障碍
- 罕见疾病 罕见疾病
背景情况:
- Pleckstrin 同源域相互作用蛋白 (PHIP) 基因中的致病变体与 Chung-Jansen 综合征有关.
- 这种综合征呈现出一系列的发育,行为和身体特征.
研究的目的:
- 描述可能具有致病性/致病性PHIP变体的个体的表型和基因型.
- 为了提供自然史数据的 - 詹森综合征,告知早期干预策略.
主要方法:
- 从47名PHIP变异个体的表型和基因型数据的回顾性分析.
- 发展延迟,行为挑战,适应性功能 (Vineland-3) 和身体症状的评估.
主要成果:
- 在61.7%的病例中,PHIP变体是de novo. 共同特征包括发育迟缓 (85.1%),低血压 (78.7%),视力问题 (66%) 和肥胖 (55.8%).
- 抑郁症和肥胖的患病率在12岁以上的人群中增加.
- 在大多数人中观察到适应性功能中度较低.
结论:
- 这个队列扩大了对 Chung-Jansen 综合征自然史的理解.
- 早期识别和干预行为,情绪和健康问题,如肥胖,对于终身管理至关重要.
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