一个由新的CHD7基因突变引起的CHARGE综合征病例报告
Yuan Zhang1, Yu Lu2, Xicui Long2
1Department of Audiology, Guizhou Provincial People's Hospital, Guiyang, China.
SAGE open medical case reports
|December 2, 2024
概括
基因检测对于诊断与CHARGE综合征相关的聋至关重要. 早期干预和多学科护理对于儿童综合征性聋管理至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 医学案例报告 病例报告
背景情况:
- 查奇综合征是一种罕见的遗传疾病,与多种先天性异常有关.
- 聋是CHARGE综合征的常见表现,影响发展和生活质量.
- 准确的基因诊断对于理解潜在机制和预后至关重要.
研究的目的:
- 报告一个具有新奇CHD7基因突变的CHARGE综合征病例.
- 强调基因检测在综合征性聋症诊断中的重要性.
- 突出早期检测和综合性聋的多学科管理的需要.
主要方法:
- 一个患有CHARGE综合征的患者的临床数据的回顾性分析.
- 受影响的孩子和父母的全基因组测序.
- 对CHD7基因突变的鉴定和致病性评估.
主要成果:
- 在该患者身上发现了CHD7基因中的一个异构的新发病性突变 (NM_017780.4:C.4853G>A,P.TP1618ter).
- 这种突变被证实是导致孩子患上CHARGE综合征的原因.
- 这些发现强调了CHD7突变在综合征性聋症中的作用.
结论:
- 基因检测,特别是全基因组测序,对于准确诊断CHARGE综合征的聋是不可或缺的.
- 早期的听力查和多学科的综合性聋的方法对于有效的早期检测,诊断,干预和康复至关重要.
- 这一案例凸显了基因洞察力在治疗复杂儿科疾病中的重要性.
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