在Dyskerine基因中的X相关的Dyskeratosis Congenita病例与突变1058C>T(p.Ala353Val)
Ayse Oktem1, Pelin Kocyigit1, Timur Tuncalı1
1From the Department of Dermatology, Medical Genetics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Indian journal of dermatology
|April 4, 2024
概括
遗传性疾病 (Dyskeratosis congenita,DC) 是一种罕见的遗传性疾病,可以在没有所有经典症状的情况下表现出来. 早期临床怀疑对于及时诊断和预防骨髓衰竭患者的严重后果至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 血液学 血液学 血液学
- 细胞生物学 细胞生物学
背景情况:
- 遗传性骨髓衰竭 (DC) 是一种罕见的遗传性骨髓衰竭综合征.
- 它的特点是口腔白血病,缩性指甲和网状皮肤色素的三位一体.
- DC也是一个端粒生物学障碍,影响细胞衰老和修复机制.
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