Tatton-Brown-Rahman Syndrome Due to a Novel DNMT3A Variant Presenting With Autism, Attention-Deficit/Hyperactivity Disorder (ADHD), and Regression: A Saudi Case Report

由新型DNMT3A变异引起的Tatton-Brown-Rahman综合征,表现为自闭症、注意力缺陷/多动障碍(ADHD)和退行性行为:沙特阿拉伯病例报告

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Abstract

Tatton-Brown-Rahman syndrome (TBRS) is a rare overgrowth/intellectual disability disorder caused by DNMT3A variants. It is characterized by tall stature, macrocephaly, and intellectual disability, with an expanding neuropsychiatric spectrum that includes autism spectrum disorder (ASD) and behavioral disturbances. We describe a young adult Saudi male with overgrowth, macrocephaly, coarse facial features, and global developmental delay. Cognitive testing confirmed mild intellectual disability with relative verbal strengths. He was diagnosed with ASD and attention-deficit/hyperactivity disorder (ADHD) and treated with methylphenidate in childhood. In early adulthood, the patient exhibited regression characterized by speech loss, decline in self-care, incontinence, and psychotic-like symptoms, alongside gastrointestinal disease. Genetic testing revealed a novel heterozygous DNMT3A missense variant (c.923G>T, p.Gly308Val) in the PWWP domain, consistent with TBRS. This case illustrates the broadened phenotype of TBRS, including ASD, ADHD, and regression, paralleling prior reports of cognitive unevenness and behavioral vulnerability. Additional findings of eczema, elevated IgE, and anemia suggest possible underrecognized systemic involvement. This case emphasizes the importance of multidisciplinary evaluation and lifelong neuropsychiatric follow-up in TBRS. As the first reported case from Saudi Arabia to our knowledge, it broadens the clinical and geographic spectrum of the disorder and highlights the association between DNMT3A variants, intellectual disability, and ASD.

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