Developmental aspects of FXAND in a man with the FMR1 premutation

Ellery Santos1,2, Chinelo Emeka-Nwonovo1, Jun Yi Wang1,3,4

  • 1MIND Institute, University of California Davis School of Medicine, Sacramento, CA, USA.

Abstract

Insights

Fragile X premutation can cause neuropsychiatric disorders (FXAND), distinct from FXTAS. This case highlights a male FMR1 carrier with autism, anxiety, and cognitive deficits, illustrating FXAND.

Area of Science:

  • Neurogenetics
  • Psychiatry
  • Developmental Neuroscience

Background:

  • The Fragile X mental retardation 1 (FMR1) premutation is linked to various neurodevelopmental issues.
  • Fragile X-associated Neuropsychiatric Disorders (FXAND) encompass conditions like autism spectrum disorder (ASD), anxiety, and ADHD.
  • FXAND are distinct from the neurodegenerative Fragile X-associated Tremor/Ataxia syndrome (FXTAS).

Observation:

  • A case study of a 26-year-old male with the FMR1 premutation presenting with depression and anxiety from age 10.
  • Evaluations at ages 13, 18, and 26 included cognitive assessments, psychiatric evaluations, and brain MRI.
  • The patient was diagnosed with autism spectrum disorder (ASD) at age 13.

Findings:

  • Cognitive assessment at age 18 revealed a full-scale IQ of 64.
  • Psychiatric evaluations confirmed social anxiety disorder, agoraphobia, and selective mutism by age 26.
  • Brain MRI showed enlarged ventricles, increased frontal subarachnoid spaces, and hypergyrification.

Implications:

  • This case exemplifies FMR1 premutation carriers experiencing significant psychiatric and cognitive challenges.
  • It underscores FXAND as a distinct clinical entity separate from FXTAS.
  • Further research into the mechanisms and management of FXAND in FMR1 premutation carriers is warranted.

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