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Neurochemistry of Metabolic Diseases - Lysosomal Storage Diseases, Phenylketonuria, and Canavan Disease (Hardcover)
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Neurochemistry of Metabolic Diseases - Lysosomal Storage Diseases, Phenylketonuria, and Canavan Disease (Hardcover)
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Metabolic disorder caused by altered levels of metabolism resulting
pathophysiological abnormalities often leads to childhood death.
Several new developments on metabolic diseases research have been
emerging. Gaucher disease is a lysosomal storage disorder caused by
glucocerebrosidase gene mutations resulting glucocerebrosidase
deficiency. Current studies show that the same gene mutations also
contribute to the Parkinson's disease. Tetrahydrobiopterin (BH4)
has been widely used in treating patients with Phenylketonuria over
a decade. Recent studies reveal that patients treated with BH4 over
one-year period showed reduced levels of serum B12, folate and iron
intake and therefore patients under chronic BH4 treatment needed to
be advised to have additional micronutrients along with BH4.
Macrocephaly was used as one of the important features to diagnose
Canavan disease. However, a recent study showing a child with
aspartoacylase gene mutation developed microcephaly. Hence, Canavan
disease phenotype can be either macrocephaly or microcephaly. These
are a few examples of recent developments on metabolic diseases
research. Therefore, this book was aimed to compose current
developments on metabolic diseases research for the use by broad
spectrum of experts including Physicians, Neuroscientists,
Neurologists, Biomedical researchers, Biochemists, Molecular
biologists, Basic Science Researchers and Medical Students.
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