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Updated: May 10, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
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Published on: September 20, 2016

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诊断Fanconi贫血:来自印度农村的一个罕见病例报告

Aashita Malik1

  • 1Pediatrics, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Cureus
|July 30, 2024
PubMed
概括

芬科尼贫血 (FA) 是一种罕见的遗传性无塑性贫血,由DNA稳定性基因突变引起. 染色体破裂研究是诊断这种具有各种症状的具有挑战性的疾病的关键.

关键词:
双手指的形指范科尼贫血症 范科尼贫血症低细胞骨髓的低细胞骨髓这种药物是mitomycin c c.脏发育的原因是脏衰老.

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