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Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report

Nicolaides-Baraitser Syndrome is a rare genetic condition that clinically presents with intellectual disabilities, facial and bone changes, and sparse hair. In Brazil, only one case has been previously reported without genetic confirmation. We present the case of an 8-year-old boy, clinically and ge...

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Autores principales: Lopes, Derek Chaves, Mendes, Lorenna Sena Teixeira, Ferreira, Inês Catão Henriques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631755/
https://www.ncbi.nlm.nih.gov/pubmed/37970954
http://dx.doi.org/10.31744/einstein_journal/2023RC0480
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author Lopes, Derek Chaves
Mendes, Lorenna Sena Teixeira
Ferreira, Inês Catão Henriques
author_facet Lopes, Derek Chaves
Mendes, Lorenna Sena Teixeira
Ferreira, Inês Catão Henriques
author_sort Lopes, Derek Chaves
collection PubMed
description Nicolaides-Baraitser Syndrome is a rare genetic condition that clinically presents with intellectual disabilities, facial and bone changes, and sparse hair. In Brazil, only one case has been previously reported without genetic confirmation. We present the case of an 8-year-old boy, clinically and genetically diagnosed with Nicolaides-Baraitser Syndrome, who developed autism spectrum disorder characteristics with a formal diagnosis at the age of eight. Diagnosing autism spectrum disorder in patients with intellectual disabilities is a clinical challenge requiring careful evaluation.
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spelling pubmed-106317552023-11-09 Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report Lopes, Derek Chaves Mendes, Lorenna Sena Teixeira Ferreira, Inês Catão Henriques Einstein (Sao Paulo) Case Report Nicolaides-Baraitser Syndrome is a rare genetic condition that clinically presents with intellectual disabilities, facial and bone changes, and sparse hair. In Brazil, only one case has been previously reported without genetic confirmation. We present the case of an 8-year-old boy, clinically and genetically diagnosed with Nicolaides-Baraitser Syndrome, who developed autism spectrum disorder characteristics with a formal diagnosis at the age of eight. Diagnosing autism spectrum disorder in patients with intellectual disabilities is a clinical challenge requiring careful evaluation. Instituto Israelita de Ensino e Pesquisa Albert Einstein 2023-10-26 /pmc/articles/PMC10631755/ /pubmed/37970954 http://dx.doi.org/10.31744/einstein_journal/2023RC0480 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lopes, Derek Chaves
Mendes, Lorenna Sena Teixeira
Ferreira, Inês Catão Henriques
Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title_full Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title_fullStr Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title_full_unstemmed Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title_short Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report
title_sort autism spectrum disorder in a patient with nicolaides-baraitser syndrome: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631755/
https://www.ncbi.nlm.nih.gov/pubmed/37970954
http://dx.doi.org/10.31744/einstein_journal/2023RC0480
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