CHEDDA syndrome: a case report and review of the literature for this newly described entity

Congenital hypotonia, epilepsy, developmental delay, and digital anomalies (CHEDDA) is a recently identified neurodevelopmental syndrome which has only 8 reported cases to date since its existence was proposed in 2007. We report a case of CHEDDA syndrome identified in a newborn female with congenita...

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Detalles Bibliográficos
Autores principales: Hui, Jessica, Kandemirli, Sedat Giray, Sato, Takashi Shawn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Neuroradiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334555/
https://www.ncbi.nlm.nih.gov/pubmed/32642015
http://dx.doi.org/10.1016/j.radcr.2020.05.079

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334555/
https://www.ncbi.nlm.nih.gov/pubmed/32642015
http://dx.doi.org/10.1016/j.radcr.2020.05.079

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