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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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Detalles Bibliográficos
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
Descripción
Sumario: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.