Prevalence of Seizure In PKU: An Analytic Historical Study

ObjectivePhenylketonuria (PKU) is an autosomal recessive metabolic genetic disorder characterized by a deficiency in the hepatic enzyme phenylalanine hydroxylase (PAH) which can cause problems with brain development, leading to progressive mental retardation, brain damage, and seizures. In this stud...

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Bibliographic Details
Main Authors: KARIMZADEH, Parvaneh, AALAEI, Mohammad Reza, RAHIMPOUR, Feisal
Format: Online
Language:eng
Published: Iranian Journal of Child Neurology 2010
Online Access:http://journals.sbmu.ac.ir/ijcn/article/view/1865

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