How Families Manage the Complex Medical Needs of Their Children with MECP2 Duplication Syndrome

MECP2 duplication syndrome (MDS) is a rare, X-linked, neurodevelopmental disorder resulting from the duplication of the methyl-CpG-binding protein 2 (MECP2) gene. The clinical features of MDS include severe intellectual disability, global developmental delay, seizures, recurrent respiratory infectio...

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Detalles Bibliográficos
Autores principales: John Cherian, Dani, Ta, Daniel, Smith, Jeremy, Downs, Jenny, Leonard, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377896/
https://www.ncbi.nlm.nih.gov/pubmed/37508699
http://dx.doi.org/10.3390/children10071202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377896/
https://www.ncbi.nlm.nih.gov/pubmed/37508699
http://dx.doi.org/10.3390/children10071202

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