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An adult patient with Tatton-Brown-Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy.

Al-Alya AlSabahMohammed AlsalmiRami MassieMarie-Claude BilodeauPhilippe M CampeauSerge McGrawMaria Daniela D'Agostino
Published in: American journal of medical genetics. Part A (2023)
Tatton-Brown-Rahman syndrome (TBRS) is a rare autosomal dominant overgrowth syndrome first reported in 2014 and caused by pathogenic variants in the DNA methyltransferase 3A (DNMT3A) gene. All individuals reported to date share a phenotype of somatic overgrowth, dysmorphic features, and intellectual disability. Peripheral neuropathy was not described in these cases. We report an adult patient with TBRS caused by a novel pathogenic DNMT3A variant (NM_175629.2: c.2036G>A, p.(Arg688His)) harboring an axonal length-dependent sensory-motor polyneuropathy. Extensive laboratory and molecular genetic work-up failed to identify alternative causes for this patient's neuropathy. We propose that axonal neuropathy may be a novel, age-dependent phenotypic feature in adults with TBRS and suggest that this syndrome should be considered in the differential diagnosis of patients with overgrowth, cognitive and psychiatric difficulties, and peripheral neuropathy.
Keyphrases
  • case report
  • intellectual disability
  • dna methylation
  • copy number
  • spinal cord injury
  • autism spectrum disorder
  • genome wide
  • machine learning
  • deep learning
  • optic nerve
  • cell free