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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Israelita de Ensino e Pesquisa Albert Einstein
2023
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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. |
format | Online Article Text |
id | pubmed-10631755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Instituto Israelita de Ensino e Pesquisa Albert Einstein |
record_format | MEDLINE/PubMed |
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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