| Literature DB >> 33683010 |
Christina G Tise1, Jose Andres Morales1, Ariel S Lee2, Frances Velez-Bartolomei1, Brendan J Floyd1, Rebecca J Levy1, Kristina P Cusmano-Ozog3, Annette S Feigenbaum2, Maura R Z Ruzhnikov1,4, Chung U Lee1, Gregory M Enns1.
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.Entities:
Keywords: Aicardi-Goutières syndrome (AGS); C26:0 lysophosphatidylcholine (C26:0-LPC); X-linked adrenoleukodystrophy (X-ALD); newborn screen (NBS); very long chain fatty acids (VLCFA)
Year: 2021 PMID: 33683010 DOI: 10.1002/ajmg.a.62160
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802