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Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
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Broad complex rhythm with a salty taste

M Boulaksil1,2, C L Meuwese3,4, R Evertz5

  • 1Department of Cardiology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands. m.boulaksil@gmail.com.

Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|January 22, 2017
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No abstract available in PubMed .

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