Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study

INTRODUCTION: Sotos Syndrome (SS, OMIM#117550) is a heterogeneous genetic condition, recognized by three main clinical features present in most cases: overgrowth with macrocephaly, typical facial appearance and different degrees of intellectual disability. Three different types are described caused...

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Detalles Bibliográficos
Autores principales: Lourdes, Vega-Hanna, Mario, Sanz-Cuesta, Didac, Casas-Alba, Mercè, Bolasell, Loreto, Martorell, Leticia, Pías, Lucia, Feller Ana, Martínez-Monseny, Antonio Federico, Mercedes, Serrano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298147/
https://www.ncbi.nlm.nih.gov/pubmed/37384309
http://dx.doi.org/10.3389/fped.2023.1184529

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298147/
https://www.ncbi.nlm.nih.gov/pubmed/37384309
http://dx.doi.org/10.3389/fped.2023.1184529

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