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

Christina G TiseJose Andres MoralesAriel S LeeFrances Velez-BartolomeiBrendan J FloydRebecca J LevyKristina P Cusmano-OzogAnnette S FeigenbaumMaura R Z RuzhnikovChung U LeeGregory M Enns
Published in: American journal of medical genetics. Part A (2021)
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.
Keyphrases
  • red blood cell
  • clinical trial
  • clinical evaluation
  • high throughput
  • case report
  • randomized controlled trial
  • public health
  • healthcare
  • single cell
  • blood brain barrier
  • single molecule
  • cord blood