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Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.
Trelles, M Pilar; Levy, Tess; Lerman, Bonnie; Siper, Paige; Lozano, Reymundo; Halpern, Danielle; Walker, Hannah; Zweifach, Jessica; Frank, Yitzchak; Foss-Feig, Jennifer; Kolevzon, Alexander; Buxbaum, Joseph.
Affiliation
  • Trelles MP; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA. pilar.trelles@mssm.edu.
  • Levy T; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA. pilar.trelles@mssm.edu.
  • Lerman B; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. pilar.trelles@mssm.edu.
  • Siper P; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Lozano R; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Halpern D; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Walker H; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Zweifach J; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Frank Y; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Foss-Feig J; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Kolevzon A; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Buxbaum J; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Mol Autism ; 12(1): 61, 2021 09 29.
Article in En | MEDLINE | ID: mdl-34588003
ABSTRACT

BACKGROUND:

FOXP1 syndrome is an autosomal dominant neurodevelopmental disorder characterized by intellectual disability, developmental delay, speech and language delays, and externalizing behaviors. We previously evaluated nine children and adolescents with FOXP1 syndrome to better characterize its phenotype. We identified specific areas of interest to be further explored, namely autism spectrum disorder (ASD) and internalizing and externalizing behaviors.

METHODS:

Here, we assess a prospective cohort of additional 17 individuals to expand our initial analyses and focus on these areas of interest. An interdisciplinary group of clinicians evaluated neurodevelopmental, behavioral, and medical features in participants. We report results from this cohort both alone, and in combination with the previous cohort, where possible.

RESULTS:

Previous observations of intellectual disability, motor delays, and language deficits were confirmed. In addition, 24% of the cohort met criteria for ASD. Seventy-five percent of individuals met DSM-5 criteria for attention-deficit/hyperactivity disorder and 38% for an anxiety disorder. Repetitive behaviors were almost universally present (95%) even without a diagnosis of ASD. Sensory symptoms, in particular sensory seeking, were common.

LIMITATIONS:

As FOXP1 syndrome is a rare disorder, sample size is limited.

CONCLUSIONS:

These findings have important implications for the treatment and care of individuals with FOXP1 syndrome. Notably, standardized testing for ASD showed high sensitivity, but low specificity, when compared to expert consensus diagnosis. Furthermore, many individuals in our cohort who received diagnoses of attention-deficit/hyperactivity disorder or anxiety disorder were not being treated for these symptoms; therefore, our findings suggest that there may be immediate areas for improvements in treatment for some individuals.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity / Autism Spectrum Disorder Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Humans Language: En Journal: Mol Autism Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity / Autism Spectrum Disorder Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Humans Language: En Journal: Mol Autism Year: 2021 Document type: Article Affiliation country: United States