在CDKN1C基因中的一种内部变异导致伊朗女孩的IMAGe综合征
Setila Dalili1, Seyyedeh Azade Hoseini Nouri1, Ameneh Sharifi2,3
1Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
这项研究在患有IMAGe综合征的儿童中发现了一种新型的内基CDKN1C变异,扩大了这种罕见疾病的已知遗传原因. 早期诊断对于管理上腺功能不全至关重要.
科学领域:
- 遗传学 遗传学 是一个
- 内分泌学 在内分泌学.
- 罕见疾病 罕见疾病
背景情况:
- IMAGe综合征是一种罕见的遗传疾病,由CDKN1C基因的病原变异引起.
- 它的特征是子宫内生长迟缓 (IUGR),甲基细胞失生症,先天性上腺失生症和生殖尿路异常.
研究的目的:
- 在被诊断患有IMAGe综合征的患者中报告一种新的内在CDKN1C变异.
- 突出整体外因子测序 (WES) 在诊断罕见遗传疾病中的重要性.
主要方法:
- 对一个具有IMAGe综合征特征的5岁伊朗女孩的临床评估.
- 整体外因子测序 (WES) 用于识别致病性遗传变异.
- 拼接AI预测和ACMG/AMP变种分类指南.
主要成果:
- 发现了一种新型异质合体内基CDKN1C变体 (c.787+4A>T),预计会破坏拼接.
- 这种变异是母性遗传的,并被归类为不确定的意义 (VUS) 的变异.
- 在相关基因中没有发现其他致病变体.
结论:
- 这一发现扩大了IMAGe综合征的遗传谱,报告了第一个内基CDKN1C变异.
- WES对于诊断至关重要;建议进行RNA分析以确认功能.
- 及时诊断对于管理可能危及生命的上腺功能衰竭至关重要.
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