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.

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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
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article

A novel de novo missense variant in ASH1L associated with mild autism spectrum disorder and an uneven cognitive profile: a case report

Romina Barros, Daura Vega-Moreno, William Nguyen, Otabek Pulatov
Journal of Medical Case Reports
Genomics and Rare Diseases
article

A novel de novo missense variant in ASH1L associated with mild autism spectrum disorder and an uneven cognitive profile: a case report

Romina Barros, Daura Vega-Moreno, William Nguyen, Otabek Pulatov
article en

Abstract

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.

Journal of Medical Case ReportsVol. 19(1)
Long Island University (US), New York University (US)
Openalex Percentile: Top 62%
Genomics and Rare Diseases
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