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A rare case of glycine encephalopathy unveiled by valproate therapy

Glycine encephalopathy (GE) or nonketotic hyperglycinemia is an autosomal recessive disorder due to a primary defect in glycine cleavage enzyme system. It is characterized by elevated levels of glycine in plasma and cerebrospinal fluid usually presenting with seizures, hypotonia, and developmental d...

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Detalles Bibliográficos
Autores principales: Subramanian, Velusamy, Kadiyala, Pramila, Hariharan, Praveen, Neeraj, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489059/
https://www.ncbi.nlm.nih.gov/pubmed/26167219
http://dx.doi.org/10.4103/1817-1745.159200