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新生儿严重联合免疫缺陷症筛查:干预的机会。

Newborn screening for severe combined immunodeficiency: an opportunity for intervention.

机构信息

Division of Hematology CHOC Children's Hospital and UC Irvine Medical Center, Orange, CA, USA.

出版信息

J Perinatol. 2013 Aug;33(8):657-8. doi: 10.1038/jp.2013.30.

Abstract

Severe combined immunodeficiency (SCID) is a potentially fatal disorder characterized by defective T- and B-lymphocyte function. We describe a 34-week female twin who had developed feeding intolerance, perioral cyanosis, abdominal distension and neutropenia at 1 month of age. Despite several evaluations including an 'inconclusive' newborn screening result for SCID, the presence of profound lymphopenia was unappreciated. Eventually a diagnosis of SCID in association with adenosine deaminase deficiency was made. This case serves to emphasize the importance of newborn screening for SCID in the context of careful evaluation of clinical and laboratory findings that may be overlooked and result in a delay in the diagnosis of a potentially life-threatening condition.

摘要

严重联合免疫缺陷症(SCID)是一种潜在致命的疾病,其特征是 T 淋巴细胞和 B 淋巴细胞功能缺陷。我们描述了一名 34 周的女性双胞胎,她在 1 个月大时出现喂养不耐受、口周发绀、腹部膨隆和中性粒细胞减少。尽管进行了多次评估,包括 SCID 的新生儿筛查结果“不确定”,但未注意到严重的淋巴细胞减少症。最终诊断为与腺苷脱氨酶缺乏相关的 SCID。该病例强调了在仔细评估临床和实验室发现的情况下,进行 SCID 新生儿筛查的重要性,这些发现可能会被忽视,并导致潜在危及生命的疾病的诊断延迟。

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