Rhabdomyolysis, acute renal failure, and cardiac arrest secondary to status dystonicus in a child with glutaric aciduria type I

Author:

Jamuar Saumya S.,Newton Stephanie A.,Prabhu Sanjay P.,Hecht Leah,Costas Karen C.,Wessel Ann E.,Harris David J.,Anselm Irina,Berry Gerard T.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. Organic acidemias due to defects in lysine oxidation: 2-ketoadipic acidemia and glutaric acidemia;Goodman,2006

2. Cerebral organic acid disorders and other disorders of lysine catabolism;Hoffman,2012

3. Type I glutaric aciduria, part 1: natural history of 77 patients;Strauss;Am. J. Med. Genet. C Semin. Med. Genet.,2003

4. Diagnosis and management of glutaric aciduria type I—revised recommendations;Kölker;J. Inherit. Metab. Dis.,2011

5. Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients;Gitiaux;Mov. Disord.,2008

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