首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Immunologic and clinical features of 25 Amish patients with RMRP 70 A-->G cartilage hair hypoplasia.
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Immunologic and clinical features of 25 Amish patients with RMRP 70 A-->G cartilage hair hypoplasia.

机译:25例RMRP 70 A→G软骨毛发发育不全的阿米什人患者的免疫学和临床特征。

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    摘要

    Cartilage-hair hypoplasia is a short limbed skeletal dysplasia associated with impairments in host-defense. To better understand the clinical heterogeneity of this disorder, we studied 25 Amish patients with homozygous mutations in RMRP (RMRP 70 A>G). Despite mutation homogeneity, eight (32%) patients had severe or recurrent infections, two (8%) of these children underwent bone-marrow transplantation for combined immunodeficiency, and the remainder were healthy. Features distinguishing patients who underwent bone marrow transplantation from others were shorter birth length, and lower serum IgG, undetectable serum IgA, and elevated circulating NK cells before 2 years of age. Irrespective of clinical phenotype, most patients had lymphopenia and reduced lymphocyte proliferation to mitogens in vitro. Our cohort analysis suggests that many patients with cartilage-hair hypoplasia are at risk for infection susceptibility particularly during the first 2 years of life. Gauging this risk is difficult, and thus careful monitoring of all patients with cartilage-hair hypoplasia is warranted.
    机译:软骨-头发发育不全是一种短肢骨骼发育不良,与宿主防御能力受损有关。为了更好地了解这种疾病的临床异质性,我们研究了25名具有RMRP纯合突变(RMRP 70 A> G)的阿米什人患者。尽管存在突变同质性,但仍有八名(32%)患者患有严重或复发性感染,其中两名(8%)儿童因合并免疫缺陷而接受了骨髓移植,其余的则健康。进行骨髓移植的患者与其他患者的区别在于出生年龄短,血清IgG降低,血清IgA不可检测以及2岁前循环NK细胞升高。无论临床表型如何,大多数患者在体外都有淋巴细胞减少症和淋巴细胞向有丝分裂原的增殖减少。我们的队列分析表明,许多患有软骨-头发发育不全的患者有感染易感性的风险,尤其是在生命的头2年。测量这种风险是困难的,因此必须对所有患有软骨-头发发育不全的患者进行仔细的监测。

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