在一个新生儿前列腺症患者中发现的FREM1和三综合症18的变异
Saima Siddiqi1, Noor Ul Ain2, Mehran Kauser2,3
1Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan. saimasiddiqi2@gmail.com.
Molecular biology reports
|July 20, 2023
概括
新生儿孕激素疾病,以过早衰老为特征,是罕见的. 这项研究确定了FREM1基因的新型变异,与新生儿前列腺症和三发症18的复杂病例有关.
科学领域:
- 遗传学 遗传学 是一个
- 罕见疾病 罕见疾病
- 儿科 儿科 儿科
背景情况:
- 新生儿前列腺体疾病具有独特的特征,如低出生体重,亡和严重的生长迟缓.
- 许多新生儿孕激素疾病病例的遗传原因仍未确定.
- 这项研究侧重于一种试验物,该试验物表现出新生儿前列腺症的标志性特征.
研究的目的:
- 为了研究一个复杂的新生儿前兆病例的遗传基础.
- 在具有新生儿前列腺特征和三症18的试验物中识别致病性遗传变异.
主要方法:
- 使用微阵列比较基因组杂交.
- 进行全外体序列测序 (WES) 来识别遗传变异.
- 桑格测序被用于变种确认.
主要成果:
- 阵列比较基因组杂交揭示了三症 18 在试验.
- 整个外体序列测序在FREM1基因中发现了新型化合物异合体变异体 (c.247 C>T; p.H83Y和c.14769868InsA).
结论:
- 呈现了一个复杂的新生儿前列腺症病例,包括心房隔膜缺陷和三症18,缺乏典型的爱德华综合征特征.
- 患者的表型与新生儿前列症一致,这表明FREM1变体是可能的原因.
- 这一案例扩大了对新生儿孕激素疾病遗传病因的理解.
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