A novel de novo missense variant in ASH1L associated with mild autism spectrum disorder and an uneven cognitive profile: a case report
This case expands the known phenotypic spectrum of ASH1L-related disorders, demonstrating that a de novo missense variant can be associated with a milder neurodevelopmental phenotype, including borderline-to-average intellectual ability. These findings challenge suggestions that missense variants uniformly lead to more severe outcomes and underscores the importance of comprehensive genomic and deep clinical characterization to refine our understanding of gene-disease relationships.
Authors
- Romina Barros
- Daura Vega-Moreno (ORCID: https://orcid.org/0000-0002-4993-4694)
- William Nguyen (ORCID: https://orcid.org/0009-0004-3594-6186)
- Otabek Pulatov (ORCID: https://orcid.org/0009-0006-7185-6908)
Institutions
- Long Island University (US)
- New York University (US)
Publication Details
- Journal
- Journal of Medical Case Reports
- Published
- 2025-11-25
- DOI
- https://doi.org/10.1186/s13256-025-05675-4
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00