部纵向缺陷 - 印度次大陆的一个独特的病例系列
Bhaskaranand Kumar1, Ashwath M Acharya2,3, S M Venugopal4
1Department of Orthopedics, Hitech Hospital, Udupi, 576103, India.
International orthopaedics
|September 25, 2024
概括
印度的腰部长度缺陷 (ULD) 显示出独特的模式,包括父母血缘关系和晚期呈现. 大多数受影响的四肢都有辐射侧手部缺陷,肘部硬和部无形成.
科学领域:
- 整形外科 整形外科 整形外科
- 遗传学 是一个遗传学.
- 儿科手术 儿科手术
背景情况:
- 长度缺陷 (ULD) 是一种罕见的先天性上肢差异.
- 在印度次大陆人口中,关于ULD的数据有限.
- 记录区域差异对于理解ULD至关重要.
研究的目的:
- 描述长度缺陷 (ULD) 的临床表现.
- 记录南亚人口中ULD独特的呈现模式.
- 为了突出该地区ULD病例的新奇性.
主要方法:
- 从2008年到2023年对医疗记录进行了回顾性病例系列分析.
- 对人口统计细节,临床特征和放射图像的全面评估.
- 基于标准肘部,前臂和手部形的患者分类.
主要成果:
- 在55名患者中记录了68只手.
- 在15%的患者中观察到血缘关系;9%的患者有家族病史的变形.
- 常见的表现包括形无形成症 (50%),固定肘部形 (41.1%),缺席第一个网络空间 (39.7%) 和缺席指 (29.4%).
- 半径侧手缺陷发生在67.6%的患者中; 62.3%的手术是因为手部形.
结论:
- 关键特征包括父母血缘关系和晚期呈现 (10岁以后).
- 大多数患者表现出辐射侧手部缺陷.
- 人们经常观察到膜无形成症和肘部硬.
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