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在卡布基综合征中新发现的轨道形:一个病例报告
Pengsen Wu1, Cheng Xiong1, Jing Rao1
1Department of Ocular Oncology and Orbital Disease, Shenzhen Eye Hospital, Jinan University, Shenzhen Eye Institute, Shenzhen, China.
European journal of ophthalmology
|April 24, 2024
概括
卡布基综合征 (KS) 是一种罕见的遗传疾病,与一种新的KMT2D基因突变有关. 这一案例突出显示了新的轨道骨形作为KS的特征特征.
科学领域:
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
- 眼科医生 眼科 眼科
背景情况:
- 卡布基综合征 (KS) 是一种罕见的遗传性疾病,其特点是有特色的面部特征,发育迟缓和器官形.
- 在KMT2D基因的突变是卡布基综合征的常见原因.
- 了解KS的遗传基础和表型谱对于诊断和管理至关重要.
研究的目的:
- 在患有卡布基综合征的患者中报告一种新的KMT2D基因突变.
- 描述该患者的临床和放射学发现,特别是轨道骨的形.
主要方法:
- 基因测序以确定KMT2D基因中的突变.
- 对特征性KS特征进行临床检查.
- 轨道计算机断层扫描 (CT) 用于评估骨结构.
主要成果:
- 在KMT2D基因中发现了一种新的突变c.11785C>T (p.Gln3929*).
- 该患者表现出典型的KS眼皮形变形:侧侧下眼皮的变形,长眼裂,超色,和中间的.
- 轨道CT检测显示了显著的轨道骨形状不良,包括移位的头骨骨,浅轨道和异常的侧壁角度,以及头骨骨和大椎形.
结论:
- 这种情况扩大了与卡布基综合征相关的KMT2D突变的范围.
- 轨道骨异常,包括肌和大椎形,是卡布基综合征的重要特征,应仔细评估.
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