临床表现 13 个儿童与alkaptonuria 的表现
Mariusz J Kujawa1, Dominik Świętoń1, Jolanta Wierzba2,3,4
12nd Department of Radiology, Medical University of Gdansk, Gdansk, Poland.
Journal of inherited metabolic disease
|July 3, 2023
概括
这项研究评估了阿尔卡普托努里亚 (AKU) 的儿童,发现暗色的尿液和关节疼痛很常见. 许多儿科AKU患者也表现出认知缺陷,强调了早期干预的必要性.
科学领域:
- 儿科罕见疾病 儿科罕见疾病
- 代谢障碍 代谢障碍 代谢障碍
- 遗传学 是一个遗传学.
背景情况:
- 阿尔卡普顿尿症 (AKU) 是一种罕见的遗传性疾病.
- 很少有研究集中在儿童早期的AKU症状上.
- 需要对儿科AKU进行全面评估.
研究的目的:
- 在儿童中全面评估早期发病的阿尔卡普顿 (AKU).
- 评估儿科AKU的临床,成像,认知和遗传方面的情况.
- 为了识别年轻AKU患者的常见症状和遗传变异.
主要方法:
- 对13名儿科AKU患者 (4-17岁) 的前性纵向研究.
- 临床评估包括色素,肌肉骨,认知和适应能力.
- 磁共振成像 (MRI),超声波 (美国) 和分子遗传分析.
主要成果:
- 阴暗的尿液 (100%),关节疼痛 (46%) 和阴暗的耳 (46%) 是最常见的.
- 在38%的患者中发现认知缺陷/适应能力问题.
- 在MRI/US上没有发生退行性膝盖变化; 一例结石病.
结论:
- 儿科AKU呈现特征性症状和潜在的认知影响.
- 早期的AKU评估应包括临床,成像和认知评估.
- 确定了常见的HGD变体和一种新的潜在致病性等位基因.
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