Megalencephaly Polymicrogyria Polydactyly Hydrocephalus (MPPH): A Case Report and Review of Literature

Megacephaly polymicrogyria, polydactyly, hydrocephalus (MPPH) is an extremely rare condition caused by a defect in the AKT3, CCND2, or PIKR2 genes. Although the prevalence of the syndrome is very low, there is a significant clinical and radiological variation in the syndrome. We present a case with...

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Detalles Bibliográficos
Autores principales: Ortiz, Juan Fernando, Ruxmohan, Samir, Khurana, Mahika, Hidalgo, Jessica, Alzamora, Ivan Mateo, Patel, Amrapali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327302/
https://www.ncbi.nlm.nih.gov/pubmed/34354878
http://dx.doi.org/10.7759/cureus.16132

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327302/
https://www.ncbi.nlm.nih.gov/pubmed/34354878
http://dx.doi.org/10.7759/cureus.16132

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