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Can Respir J. 2014 Jan-Feb;21(1):17-9. doi: 10.1155/2014/404506. Epub 2013 Nov 28.
2
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本文引用的文献

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The long quest for neonatal screening for severe combined immunodeficiency.新生儿严重联合免疫缺陷症筛查的漫长探索。
J Allergy Clin Immunol. 2012 Mar;129(3):597-604; quiz 605-6. doi: 10.1016/j.jaci.2011.12.964. Epub 2012 Jan 24.
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Screening newborns for primary T-cell immunodeficiencies: consensus and controversy.新生儿原发性 T 细胞免疫缺陷的筛查:共识与争议。
Expert Rev Clin Immunol. 2011 Nov;7(6):761-8. doi: 10.1586/eci.11.25.
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Systematic evidence review of newborn screening and treatment of severe combined immunodeficiency.新生儿严重联合免疫缺陷的筛查和治疗的系统证据回顾。
Pediatrics. 2010 May;125(5):e1226-35. doi: 10.1542/peds.2009-1567. Epub 2010 Apr 19.
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CD3 deficiencies.CD3缺陷
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Effect of CD3delta deficiency on maturation of alpha/beta and gamma/delta T-cell lineages in severe combined immunodeficiency.CD3δ缺陷对重症联合免疫缺陷中α/β和γ/δ T细胞谱系成熟的影响。
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6
Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival.新生儿期严重联合免疫缺陷的造血干细胞移植可带来更好的胸腺输出并提高生存率。
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7
Early diagnosis of severe combined immunodeficiency syndrome.严重联合免疫缺陷综合征的早期诊断
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8
European experience of bone-marrow transplantation for severe combined immunodeficiency.欧洲严重联合免疫缺陷病骨髓移植的经验
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两家系严重联合免疫缺陷在一家三级中心的呼吸表现,突出了认识这种儿科急症的重要性。

The respiratory presentation of severe combined immunodeficiency in two Mennonite children at a tertiary centre highlighting the importance of recognizing this pediatric emergency.

出版信息

Can Respir J. 2014 Jan-Feb;21(1):17-9. doi: 10.1155/2014/404506. Epub 2013 Nov 28.

DOI:10.1155/2014/404506
PMID:24288697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3938231/
Abstract

Severe combined immunodeficiency (SCID) is considered to be a pediatric emergency, with respiratory distress being the most common presenting symptom. The authors present two cases of SCID in children <4 months of age with respiratory distress at a tertiary care centre due to a recently described homozygous CD3 delta mutation found only in the Mexican Mennonite population. Failure to respond to broad-spectrum antibiotics prompted investigation for possible SCID. Bronchial alveolar lavage fluid from both patients grew Pneumocystis jiroveci, and flow cytometry revealed absent T cells. The CD3 delta gene is believed to be important in T cell differentiation and maturation. The present article reminds pediatricians and pediatric respirologists that the key to diagnosing SCID is to have a high index of suspicion if there is poor response to conventional therapies.

摘要

严重联合免疫缺陷症(SCID)被认为是一种儿科急症,以呼吸窘迫为最常见的表现症状。作者介绍了在一家三级保健中心,因呼吸窘迫就诊的 2 例<4 月龄的儿童 SCID 病例,其呼吸窘迫的原因是最近在仅存在于墨西哥门诺派人群中的纯合 CD3 delta 突变。由于对广谱抗生素治疗反应不佳,故对可能的 SCID 进行了检查。这 2 例患者的支气管肺泡灌洗液均生长卡氏肺囊虫,流式细胞术显示 T 细胞缺失。CD3 delta 基因被认为在 T 细胞分化和成熟中起重要作用。本文提醒儿科医生和儿童呼吸科医生,诊断 SCID 的关键是如果对常规治疗反应不佳,要高度怀疑 SCID。