糖原储存障碍型IXb:探索临床模式和遗传洞察力,对罕见的酸酶激酶B (PHKB) 相关病例进行研究

Inuganti Venkata Renuka1, Sudhakar Ramamoorthy1, Vijayalakshmi B2

  • 1Pathology, NRI Medical College, Chinakakani, IND.

Cureus
|August 27, 2024
PubMed
概括

本案例报告详细介绍了PHKB基因中罕见的删除突变,导致糖原储存疾病型IXb (GSD IXb). 这项研究强调了GSD IXb的遗传多样性,强调了个性化诊断.

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