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Aicardi-Goutières 综合征可能会导致新生儿 X 连锁肾上腺脑白质营养不良的筛查呈阳性。

Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophy.

机构信息

Division of Medical Genetics, Department of Pediatrics, Lucile Packard Children's Hospital and Stanford University, Stanford, California, USA.

Division of Medical Genetics, Department of Pediatrics, Rady Children's Hospital and University of California, San Diego, California, USA.

出版信息

Am J Med Genet A. 2021 Jun;185(6):1848-1853. doi: 10.1002/ajmg.a.62160. Epub 2021 Mar 8.

Abstract

We report three unrelated probands, two male and one female, diagnosed with Aicardi-Goutières syndrome (AGS) after screening positive on California newborn screening (CA NBS) for X-linked adrenoleukodystrophy (X-ALD) due to elevated C26:0 lysophosphatidylcholine (C26:0-LPC). Follow-up evaluation was notable for elevated C26:0, C26:1, and C26:0/C22:0 ratio, and normal red blood cell plasmalogens levels in all three probands. Diagnoses were confirmed by molecular sequencing prior to 12 months of age after clinical evaluation was inconsistent with X-ALD or suggestive of AGS. For at least one proband, the early diagnosis of AGS enabled candidacy for enrollment into a therapeutic clinical trial. This report demonstrates the importance of including AGS on the differential diagnosis for individuals who screen positive for X-ALD, particularly infants with abnormal neurological features, as this age of onset would be highly unusual for X-ALD. While AGS is not included on the Recommended Universal Screening Panel, affected individuals can be identified early through state NBS programs so long as providers are aware of a broader differential that includes AGS. This report is timely, as state NBS algorithms for X-ALD are actively being established, implemented, and refined.

摘要

我们报告了三例无关的先证者,两男一女,在加利福尼亚新生儿筛查(CA NBS)中因 X 连锁肾上腺脑白质营养不良(X-ALD)呈阳性而被诊断为 Aicardi-Goutières 综合征(AGS),原因是 C26:0 溶血磷脂酰胆碱(C26:0-LPC)升高。所有三个先证者的随访评估均显示 C26:0、C26:1 和 C26:0/C22:0 比值升高,红细胞质体素水平正常。在临床评估与 X-ALD 不一致或提示 AGS 之前,在 12 个月龄之前通过分子测序确认了诊断。对于至少一个先证者,AGS 的早期诊断使其有资格参加治疗性临床试验。本报告表明,对于 X-ALD 筛查呈阳性的个体,特别是具有异常神经特征的婴儿,将 AGS 纳入鉴别诊断非常重要,因为这种发病年龄对于 X-ALD 来说非常罕见。虽然 AGS 未包含在推荐的通用筛查面板中,但只要提供者了解包括 AGS 在内的更广泛的鉴别诊断,就可以通过州 NBS 计划尽早识别出受影响的个体。由于 X-ALD 的州 NBS 算法正在积极建立、实施和完善,因此本报告非常及时。

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