Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report

BACKGROUND: We described the main features of an infant diagnosed with facial dysmorphic, language failure, intellectual disability and congenital malformations to strengthen our understanding of the disease. Currently, treatment is only rehabilitation and surgery for cleft lip and palate. CASE SUMM...

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Detalles Bibliográficos
Autores principales: Toral-Lopez, Jaime, Huerta, Luz María González, Messina-Baas, Olga, Cuevas-Covarrubias, Sergio A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674752/
https://www.ncbi.nlm.nih.gov/pubmed/33269262
http://dx.doi.org/10.12998/wjcc.v8.i21.5296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674752/
https://www.ncbi.nlm.nih.gov/pubmed/33269262
http://dx.doi.org/10.12998/wjcc.v8.i21.5296

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