自体递归肢体腰带肌肉缩5型 (LGMDR-5)
Hamritha Ashokkumar1, Sakshi Upendra Bhatia1, Vaanmathi Azhagar Nambi Santhi2
1Department of Paediatrics, SIMATS Deemed University, Saveetha Medical College and Hospital, Chennai, Tamil Nadu, India.
BMJ case reports
|May 27, 2024
概括
这项研究详细介绍了一种罕见的四肢腰带肌肉发育不良 (LGMD) 病例,特别是以前命名为LGMD2C,现在被称为LGMDR5. 临床外基因组测序证实了一名青少年男性的遗传诊断,他呈现出肢体逐渐疲软.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 罕见疾病 罕见疾病
背景情况:
- 肢体腰带肌肉发育不良 (LGMD) 是一组罕见的遗传肌肉疾病.
- 它的特点是渐进的软弱和缩,主要发生在肩膀和骨盆腰带.
研究的目的:
- 报告一种罕见的自体逆行性LGMD病例.
- 突出特定LGMD亚型的诊断过程和遗传确认.
主要方法:
- 一个青少年男性的临床表现和检查,其肢体软弱进展.
- 通过临床外体序列测序证实了诊断.
- 鉴定一种罕见的LGMD亚型的致病变体.
主要成果:
- 患者呈现出近端肌肉消耗,缩,低血压和四个四肢的功率下降.
- 观测到高尔的标志和头巾翅膀的翅膀.
- 临床外基因组测序揭示了一种致病性变体,与自身逆性LGMD一致,此前称为LGMD2C,现在称为LGMDR5.
结论:
- 这一案例凸显了基因测试在诊断罕见形式的LGMD方面的重要性.
- 通过外基因组测序进行准确的诊断对于理解和管理LGMDR5 (以前的LGMD2C) 是至关重要的.
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