Microdeletion 3q13.33-3q21.2: A Rare Cause of Neurodevelopmental Disorder

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1De Novo 3q27.1 Microdeletion Refines the Critical Region and Implicates PSMD2 Haploinsufficiency in Growth and Neurodevelopmental Abnormalities.2026
2. 2Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a <i>de novo</i> Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat2026
3. 3Expanding the Clinical Spectrum of De Novo 19p13.3 Microdeletion: A Case Report2025
4. 4Case Report: developmental delay and intellectual disability linked to a maternally inherited derivative chromosome 3 from a t(3;8) translocation2025
5. 5Late diagnosis of a 3p26.3p25.2 microduplication in a young adult with mild neurodevelopmental features: a case report and literature review2026