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Updated: Sep 19, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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婴儿补充剂失调:一个CD59缺乏病例与神经后果

Fadi Busaleh1, Heeba Y Al Kalaf2, Nabil Almajhad3

  • 1Pediatric, Maternity and Children's Hospital, Al-Ahsa, SAU.

Cureus
|June 16, 2025
PubMed
概括

CD59缺乏症是一种罕见的遗传性疾病,会导致严重的并发症,如中风和血液溶解. 早期诊断和补充抑制对于治疗婴儿这种疾病至关重要.

关键词:
剧烈的松性麻急性麻cd59 缺陷 缺陷 缺陷 缺陷免疫血液溶解性贫血 免疫血液溶解性贫血婴儿低血压症 在婴儿时期的低血压症.婴儿中风 婴儿中风非免疫性血液溶解性贫血症性夜间血液溶解性贫血症.

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