Sjogren-Larsson syndrome brain volumetric reductions demonstrated with an automated software

Background  Sjogren-Larsson syndrome (SLS) is a neurocutaneous disease with an autosomal recessive inheritance, caused by mutations in the gene that encodes fatty aldehyde dehydrogenase ( ALDH3A2 ), clinically characterized by ichthyosis, spastic diplegia, and cognitive impairment. Brain imaging pla...

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Detalles Bibliográficos
Autores principales: Castro, José Thiago de Souza de, Saab, Camilo Lotfi, Souto, Mariam Patrícia Auada, Ortolam, Juliane Giselle, Steiner, Carlos Eduardo, Rezende, Thiago Junqueira Ribeiro de, Reis, Fabiano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Revinter Publicações Ltda. 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10550349/
https://www.ncbi.nlm.nih.gov/pubmed/37793403
http://dx.doi.org/10.1055/s-0043-1772601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10550349/
https://www.ncbi.nlm.nih.gov/pubmed/37793403
http://dx.doi.org/10.1055/s-0043-1772601

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