Delayed Recognition and Stroke-Predominant Presentation in Down Syndrome–Associated Moyamoya Syndrome
BACKGROUND: Children with Down syndrome (DS) are at high risk for moyamoya syndrome (MMS) and ischemic stroke, yet early detection strategies remain poorly defined despite the condition being surgically treatable. METHODS: We conducted a multicenter retrospective cohort study comparing children with Down syndrome–associated moyamoya syndrome (DS-MMS) and MMS without DS (MMS). The primary outcome was stroke as the primary presenting symptom. Secondary outcomes included diagnostic delays, angiographic features, prediagnostic systolic blood pressure percentiles, and 1-year neurological outcomes. Multivariable models adjusted for demographic and access-related covariates. RESULTS: In total, 271 patients were identified; 198 (73.1%) met inclusion criteria and comprised the analytic cohort. Among 198 patients (77 DS-MMS; 121 MMS), DS-MMS mean age was 9.5±5.2 years (50.6% female), and MMS mean age was 7.4±3.0 years (54.5% female). Stroke at presentation was more common in DS-MMS (71.4% versus 20.7%; absolute difference, 50.7%), corresponding to an adjusted odds ratio of 14.50 ([95% CI, 6.65–31.60]; P <0.001). Children with DS-MMS experienced longer delays from symptom onset to presentation and from presentation to diagnostic confirmation (both P <0.001). Posterior circulation involvement was more frequent in DS-MMS (adjusted odds ratio, 2.18 [95% CI, 1.09–4.37]; P =0.03), whereas angiographic severity was similar between groups. In the prediagnostic period, DS-MMS demonstrated a progressive rise in systolic blood pressure percentiles, exceeding the MMS cohort by 6 months ( P <0.001). At 1 year, DS-MMS was associated with greater disability (adjusted odds ratio, 2.58 [95% CI, 1.45–4.57]; P <0.001) and spasticity (adjusted odds ratio, 6.33 [95% CI, 3.12–12.83]; P <0.001). CONCLUSIONS: DS-MMS represents a high-risk cerebrovascular phenotype characterized by delayed recognition and a markedly increased likelihood of stroke at presentation. Rising blood pressure percentiles preceding diagnosis may serve as an early physiological signal. These findings support targeted early detection strategies and a lower threshold for vascular imaging in symptomatic patients.
Authors
- Anthony Wang (ORCID: https://orcid.org/0000-0002-9509-6257)
- Gary K. Steinberg (ORCID: https://orcid.org/0000-0001-6374-1058)
- Michael S. Rafii (ORCID: https://orcid.org/0000-0003-2640-2094)
- Jonathan Douglas Santoro (ORCID: https://orcid.org/0000-0002-8350-8234)
- Elizabeth W. Mayne (ORCID: https://orcid.org/0000-0002-5959-7134)
- Deepti Nagesh (ORCID: https://orcid.org/0000-0002-4928-0782)
- Mackenzie Silverman
- Brian G. Skotko (ORCID: https://orcid.org/0000-0002-5232-9882)
- Sarah Lee (ORCID: https://orcid.org/0000-0002-8821-6636)
- M N Yousuf
- Maeve C. Lucas (ORCID: https://orcid.org/0009-0007-4802-3788)
- Samuel T. Otey (ORCID: https://orcid.org/0009-0000-2689-9841)
- Eugenia Ho
Institutions
- University of Southern California (US)
- Children's Hospital of Los Angeles (US)
- Harvard University (US)
- University of California, Los Angeles (US)
- Southern States University (US)
- Stanford University (US)
Publication Details
- Journal
- Stroke
- Published
- 2026-07-24
- DOI
- https://doi.org/10.1161/strokeaha.126.056969
- Primary Topic
- Moyamoya disease diagnosis and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00