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x-linked scid

/ˈeks lɪŋkt skɪd/

翻译: X连锁严重联合免疫缺陷病是一种由X染色体上IL2RG基因突变引起的原发性免疫缺陷病,导致功能性T细胞和自然杀伤细胞缺失,使患者从出生起就极易发生严重感染。

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/ˈeks lɪŋkt skɪd/formalmedical
  • zhX连锁严重联合免疫缺陷病是一种由X染色体上IL2RG基因突变引起的原发性免疫缺陷病,导致功能性T细胞和自然杀伤细胞缺失,使患者从出生起就极易发生严重感染。

A severe combined immunodeficiency disorder caused by a mutation in the IL2RG gene on the X chromosome, resulting in a lack of functional T cells and natural killer cells, leading to severe vulnerability to infections from birth.

  1. Severe Combined ImmunodeficiencyC2formal

    A rare genetic disorder affecting the immune system, caused by a mutation on the X chromosome, leading to severe infections.

    zhX连锁重症联合免疫缺陷病

    • X-linked SCID is often diagnosed in infancy due to recurrent infections.
    • Gene therapy has shown promise in treating X-linked SCID.
    • Babies with X-linked SCID require immediate medical intervention.