Adjuvant Treatment for Protocadherin 19 (PCDH19) Syndrome

Protocadherin 19 (PCDH19) syndrome is inherited as an X-linked pattern and affects mainly females. This syndrome is caused by a mutation in the PCDH19 gene encoding for the protocadherin protein. It is characterized by refractory seizures during febrile episodes with neuropsychiatric manifestations....

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Detalles Bibliográficos
Autores principales: Moncayo, Juan A, Vargas, Maite N, Castillo, Isabel, Granda, Pablo V, Duque, Andrea M, Argudo, Jennifer M, Matcheswalla, Sakina, Lopez Dominguez, Guillermo E, Monteros, Gustavo, Andrade, Andres F, Ojeda, Diego, Yepez, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392850/
https://www.ncbi.nlm.nih.gov/pubmed/36004035
http://dx.doi.org/10.7759/cureus.27154

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392850/
https://www.ncbi.nlm.nih.gov/pubmed/36004035
http://dx.doi.org/10.7759/cureus.27154

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