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Developmental aspects of FXAND in a man with the FMR1 premutation

BACKGROUND: Fragile X mental retardation 1 (FMR1) premutation can cause developmental problems including autism spectrum disorder (ASD), social anxiety, depression, and attention deficit hyperactivity disorder (ADHD). These problems fall under an umbrella term of Fragile X‐associated Neuropsychiatri...

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Autores principales: Santos, Ellery, Emeka‐Nwonovo, Chinelo, Wang, Jun Yi, Schneider, Andrea, Tassone, Flora, Hagerman, Paul, Hagerman, Randi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005639/
https://www.ncbi.nlm.nih.gov/pubmed/31899609
http://dx.doi.org/10.1002/mgg3.1050
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author Santos, Ellery
Emeka‐Nwonovo, Chinelo
Wang, Jun Yi
Schneider, Andrea
Tassone, Flora
Hagerman, Paul
Hagerman, Randi
author_facet Santos, Ellery
Emeka‐Nwonovo, Chinelo
Wang, Jun Yi
Schneider, Andrea
Tassone, Flora
Hagerman, Paul
Hagerman, Randi
author_sort Santos, Ellery
collection PubMed
description BACKGROUND: Fragile X mental retardation 1 (FMR1) premutation can cause developmental problems including autism spectrum disorder (ASD), social anxiety, depression, and attention deficit hyperactivity disorder (ADHD). These problems fall under an umbrella term of Fragile X‐associated Neuropsychiatric Disorders (FXAND) and is separate from Fragile X‐associated Tremor/Ataxia syndrome (FXTAS), a neurodegenerative disorder. METHODS/CLINICAL CASE: A 26‐year‐old Caucasian male with the Fragile X premutation who presented with multiple behavior and emotional problems including depression and anxiety at 10 years of age. He was evaluated at 13, 18, and 26 years old with age‐appropriate cognitive assessments, psychiatric evaluations, and an MRI of the brain. RESULTS: The Autism Diagnostic Observation Scale (ADOS) was done at 13 years old and showed the patient has autism spectrum disorder (ASD). An evaluation at 18 years old showed a full‐scale IQ of 64. A Kiddie Schedule for Affective Disorders and Schizophrenia (K‐SADS) performed at 26 years old confirmed the previous impression of social anxiety disorder, agoraphobia disorder, and selective mutism. His MRI acquired at 26 years old showed enlarged ventricles, increased frontal subarachnoid spaces, and hypergyrification. CONCLUSION: This is an exemplary case of an FMR1 premutation carrier with significant psychiatric and cognitive issues that demonstrates Fragile X‐associated Neuropsychiatric Disorders (FXAND) as separate from the other well‐known premutation disorders.
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spelling pubmed-70056392020-02-13 Developmental aspects of FXAND in a man with the FMR1 premutation Santos, Ellery Emeka‐Nwonovo, Chinelo Wang, Jun Yi Schneider, Andrea Tassone, Flora Hagerman, Paul Hagerman, Randi Mol Genet Genomic Med Clinical Reports BACKGROUND: Fragile X mental retardation 1 (FMR1) premutation can cause developmental problems including autism spectrum disorder (ASD), social anxiety, depression, and attention deficit hyperactivity disorder (ADHD). These problems fall under an umbrella term of Fragile X‐associated Neuropsychiatric Disorders (FXAND) and is separate from Fragile X‐associated Tremor/Ataxia syndrome (FXTAS), a neurodegenerative disorder. METHODS/CLINICAL CASE: A 26‐year‐old Caucasian male with the Fragile X premutation who presented with multiple behavior and emotional problems including depression and anxiety at 10 years of age. He was evaluated at 13, 18, and 26 years old with age‐appropriate cognitive assessments, psychiatric evaluations, and an MRI of the brain. RESULTS: The Autism Diagnostic Observation Scale (ADOS) was done at 13 years old and showed the patient has autism spectrum disorder (ASD). An evaluation at 18 years old showed a full‐scale IQ of 64. A Kiddie Schedule for Affective Disorders and Schizophrenia (K‐SADS) performed at 26 years old confirmed the previous impression of social anxiety disorder, agoraphobia disorder, and selective mutism. His MRI acquired at 26 years old showed enlarged ventricles, increased frontal subarachnoid spaces, and hypergyrification. CONCLUSION: This is an exemplary case of an FMR1 premutation carrier with significant psychiatric and cognitive issues that demonstrates Fragile X‐associated Neuropsychiatric Disorders (FXAND) as separate from the other well‐known premutation disorders. John Wiley and Sons Inc. 2020-01-03 /pmc/articles/PMC7005639/ /pubmed/31899609 http://dx.doi.org/10.1002/mgg3.1050 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Reports
Santos, Ellery
Emeka‐Nwonovo, Chinelo
Wang, Jun Yi
Schneider, Andrea
Tassone, Flora
Hagerman, Paul
Hagerman, Randi
Developmental aspects of FXAND in a man with the FMR1 premutation
title Developmental aspects of FXAND in a man with the FMR1 premutation
title_full Developmental aspects of FXAND in a man with the FMR1 premutation
title_fullStr Developmental aspects of FXAND in a man with the FMR1 premutation
title_full_unstemmed Developmental aspects of FXAND in a man with the FMR1 premutation
title_short Developmental aspects of FXAND in a man with the FMR1 premutation
title_sort developmental aspects of fxand in a man with the fmr1 premutation
topic Clinical Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005639/
https://www.ncbi.nlm.nih.gov/pubmed/31899609
http://dx.doi.org/10.1002/mgg3.1050
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