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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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Utilidad diagnóstica y clínica de la secuenciación del exoma y la microanálisis del cromosoma en niños con GDD/DI: un

Maliwan Tengsujaritkul¹, Orawan Louthrenoo¹, Narueporn Likhitweerawong¹

¹Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Annals of medicine

|December 31, 2025

Abstracto

Background:

Global developmental delay/intellectual disability (GDD/ID) is among the most common neurodevelopmental disorders, with up to half of cases are attributed to genetic factors. Chromosome microarray (CMA) has traditionally been the primary genetic test for idiopathic GDD/ID. However, whole exome sequencing (WES) and whole genome sequencing (WGS) have recently emerged, substantially increasing diagnostic yields in these populations.

Methods:

We conducted a comprehensive literature search of PubMed, Scopus, EMBASE, and the Cochrane Library from inception to April 29, 2025. Studies reporting the diagnostic utility of these tests in children with GDD/ID were included and analyzed.

Results:

A total of 102 studies, comprising 55,752 children, were reviewed. The pooled diagnostic yield of WES was 0.37 (95% CI: 0.33-0.41; I² = 93%), significantly higher than that of CMA at 0.19 (95% CI: 0.16-0.21; I² = 95%). Subgroup analyses showed that WES yielded significantly higher diagnostic rates than CMA in both same-sample comparisons (OR = 2.27, 95% CI: 1.08-4.78) and different-sample comparisons (OR = 1.65, 95% CI: 1.15-2.37). Only one study evaluated WGS, reporting a diagnostic yield of 0.27. Meta-regression revealed a significant association between CMA diagnostic yield and the proportion of male participants (p < 0.01), but not with WES. No significant difference in diagnostic utility was observed between isolated GDD/ID and GDD/ID with comorbidities.

Conclusion:

In children with unexplained GDD/ID, WES demonstrates superior diagnostic and clinical utility compared to CMA. Incorporating WES as a first-line investigation in the diagnostic evaluation of GDD/ID may be warranted.

Palabras clave:

rendimiento diagnóstico secuenciación del exoma pruebas genéticas retraso global del desarrollo discapacidad intelectual

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