Glutaric aciduria type I: ultrasonographic demonstration of early signs

Glutaric aciduria type I (GA-I) is a rare inherited metabolic disease with increased excretion of glutaric acid and its metabolites. Diagnosis is often delayed until the onset of irreversible neurological deficits.

Saved in:

Bibliographic Details
Main Authors:	Forstner, Rosemarie (Author) , Hoffmann, Georg F. (Author) , Gassner, Ingemar (Author) , Heideman, Peter (Author) , De Klerk, Johannis B. C. (Author) , Lawrenz-Wolf, Burghard (Author) , Doringer, Ernst (Author) , Weiß-Wichert, Peter (Author) , Tröger, Jochen (Author) , Colombo, Jean P. (Author) , Plöchl, Engelbert (Author)
Format:	Article (Journal)
Language:	English
Published:	01 January 1999
In:	Pediatric radiology Year: 1999, Volume: 29, Issue: 2, Pages: 138-143
ISSN:	1432-1998
DOI:	10.1007/s002470050558
Online Access:	Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1007/s002470050558 Verlag, lizenzpflichtig, Volltext: https://link.springer.com/article/10.1007/s002470050558
Author Notes:	Rosemarie Forstner, Georg F. Hoffmann, Ingemar Gassner, Peter Heideman, Johannis B.C. De Klerk, Burghard Lawrenz-Wolf, Ernst Doringer, Peter Weiß-Wichert, Jochen Tröger, Jean P. Colombo, Engelbert Plöchl

Description
Summary:	Glutaric aciduria type I (GA-I) is a rare inherited metabolic disease with increased excretion of glutaric acid and its metabolites. Diagnosis is often delayed until the onset of irreversible neurological deficits.
Item Description:	Gesehen am 22.01.2021
Physical Description:	Online Resource
ISSN:	1432-1998
DOI:	10.1007/s002470050558