相关实验视频
Updated: Jul 6, 2025

06:31
Transuterine Fetal Tracheal Occlusion Model in Mice
Published on: February 5, 2021
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家族性先天性喉支气管狭窄症:一个系统性审查
Jeyasakthy Saniasiaya1, Graeme van der Meer2, Ed C Toll2
1Department of Otorhinolaryngology, Starship Children's Hospital, Te Whatu Ora Te Toka Tumai, Auckland, New Zealand; Department of Otorhinolaryngology, Faculty of Medicine, University of Malaya, Malaysia.
International journal of pediatric otorhinolaryngology
|January 5, 2024
概括
家族性先天性喉肌狭窄症 (FCLS) 影响新生儿,女性双胞胎的发病率为100%. 血缘关系,双胞胎出生和女性性别可能会使个人容易患上这种罕见的疾病.
科学领域:
- 儿科耳鼻喉科 儿科耳鼻喉科
- 遗传学 是一个遗传学.
- 新生儿医学 新生儿医学
背景情况:
- kongenital laryngotracheal stenosis (CLS) 是一种罕见的新生儿疾病,会导致.
- 家庭病例 (FCLS) 表明存在遗传因素.
- 了解FCLS病理生理学对于向治疗至关重要.
结论:
- 血缘关系,双胞胎出生和女性性别是FCLS的潜在诱导因素.
- 由于FCLS的罕见性限制了当前证据的质量.
- 需要进一步的研究来阐明FCLS的遗传基础.
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