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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...
Autores principales: | Ortiz, Juan Fernando, Ruxmohan, Samir, Khurana, Mahika, Hidalgo, Jessica, Alzamora, Ivan Mateo, Patel, Amrapali |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
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 |
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