Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan and Claypool Publishers, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan and Claypool Publishers, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Biota Publishing, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Biota Publishing 2013-03, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Morgan & Claypool Publishers, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Verlag: Biota Publishing, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - X-linked adrenoleukodystrophy (X-ALD) is the most common leukodystrophy and the most frequent peroxisomal disorder, with an estimated incidence of 1:17,000. This complex neurodegenerative disorder is characterized by a huge clinical variability both in the age of onset and in symptoms. The two main forms are the childhood cerebral ALD (ccALD) characterized by inflammatory demyelination of the central nervous system, and the adult form called adrenomyeloneuropathy (AMN), characterized by a non-inflammatory slowly progressive demyelination affecting spinal cord and peripheral nerves. Adrenal insufficiency is usually associated with the nervous symptoms, X-ALD being the main cause of Addison's disease. The main biochemical defect is the accumulation of very-long-chain fatty acids (VLCFA, fatty acids with a chain length of more than 22 carbon atoms), particularly in the cholesterol ester fraction of the adrenal gland and brain white matter. X-ALD is associated with mutations in the ABCD1 gene, which encodes for a peroxisomal ATPBinding Cassette (ABC) transporter predicted to allow VLCFA-CoA to enter into the peroxisome for their -oxidation. In spite of animal models, the physiopathogenesis of the disease remains poorly understood. However, several therapeutic strategies have been investigated. Among them, allogeneic bone marrow transplantation has proven effective and, more recently, the first gene therapy trial ended with a resounding success.
Verlag: Biota Publishing, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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Kartoniert / Broschiert. Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. X-linked adrenoleukodystrophy (X-ALD) is the most common leukodystrophy and the most frequent peroxisomal disorder, with an estimated incidence of 1:17,000. This complex neurodegenerative disorder is characterized by a huge clinical variability both in the .
Verlag: Morgan & Claypool Life Sciences, 2013
ISBN 10: 1615045546 ISBN 13: 9781615045549
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