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新生儿炎症性皮肤和肠道疾病1 (NISBD1):一个ADAM17同卵性突变病例
Hannah R Chang1, Megan Bannon2, Chloe Opper2
1University of Texas Southwestern Medical School, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
新生儿炎症性皮肤和肠道疾病1 (NISBD1) 是一种罕见的遗传疾病. 在一个患有严重皮肤和胃肠道症状的婴儿身上发现了一种新的ADAM17突变,证实了NISBD1的诊断.
科学领域:
- 遗传学 遗传学是一种遗传学.
- 皮肤病学 皮肤病学
- 儿科 儿科 儿科
背景情况:
- 新生儿炎症性皮肤和肠道疾病1 (NISBD1) 是一种罕见的自体遗传性衰退性疾病.
- 它是由ADAM17基因的突变引起的.
- 临床特征包括慢性腹,发育不良,皮疹和反复出现的细菌感染.
研究的目的:
- 在一个6周大的婴儿身上呈现NISBD1病例.
- 为了确定婴儿症状的遗传原因.
- 通过基因检测来确认NISBD1的诊断.
主要方法:
- 对一个6周大的男婴进行临床检查,该婴儿出现了疹喷发,腹和发育不良.
- 基因测试用于识别ADAM17基因中的突变.
主要成果:
- 婴儿呈现出分散的红色,焦点侵蚀,疹喷发,慢性腹,以及无法壮成长.
- 基因测试揭示了一种新型的,同卵性致病性ADAM17变体 (p.(Glu150=):c.450G>A).
- 这种变体被证实会破坏接捐赠部位.
结论:
- 鉴定到的ADAM17变种证实了NISBD1.1的诊断.
- 这一案例扩大了对ADAM17突变及其在NISBD1.1中的作用的理解.
- 强调基因检测对于诊断罕见新生儿疾病的重要性.
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