Clinical and neurocognitive outcome in symptomatic isovaleric acidemia

Despite its first description over 40 years ago, knowledge of the clinical course of isovaleric acidemia (IVA), a disorder predisposing to severe acidotic episodes during catabolic stress, is still anecdotal. We aimed to investigate the phenotypic presentation and factors determining the neurologica...

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Bibliographic Details
Main Authors: Grünert, Sarah (Author) , Lindner, Martin (Author) , Leichsenring, Michael (Author)
Format: Article (Journal)
Language:English
Published: 2012
In: Orphanet journal of rare diseases
Year: 2012, Volume: 7
ISSN:1750-1172
DOI:10.1186/1750-1172-7-9
Online Access:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1186/1750-1172-7-9
Verlag, kostenfrei, Volltext: https://doi.org/10.1186/1750-1172-7-9
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Author Notes:Sarah C. Grünert, Udo Wendel, Martin Lindner, Michael Leichsenring, K. Otfried Schwab, Jerry Vockley, Willy Lehnert and Regina Ensenauer
Description
Summary:Despite its first description over 40 years ago, knowledge of the clinical course of isovaleric acidemia (IVA), a disorder predisposing to severe acidotic episodes during catabolic stress, is still anecdotal. We aimed to investigate the phenotypic presentation and factors determining the neurological and neurocognitive outcomes of patients diagnosed with IVA following clinical manifestation.
Item Description:Published: 25 January 2012
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Physical Description:Online Resource
ISSN:1750-1172
DOI:10.1186/1750-1172-7-9