Volume 41, Issue 3 pp. 404-407
Brief Communication
Full Access

Use of desferrioxamine in the treatment of aceruloplasminemia

Hiroaki Miyajima MD

Hiroaki Miyajima MD

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Yoshitomo Takahashi MD

Yoshitomo Takahashi MD

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Tadashi Kamata MD

Tadashi Kamata MD

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Hideaki Shimizu MD

Hideaki Shimizu MD

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Naoki Sakai MD

Naoki Sakai MD

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan

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Dr. Jonathan D. Gitlin MD

Corresponding Author

Dr. Jonathan D. Gitlin MD

Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO

Washington University School of Medicine, Department of Pediatrics, St. Louis Children's Hospital, One Children's Place, St. Louis, MO 63110Search for more papers by this author
First published: 08 October 2004
Citations: 147

Abstract

Aceruloplasminemia is a newly recognized autosomal recessive disorder of iron metabolism resulting in neurodegeneration of the retina and basal ganglia. We report here on the treatment of a patient who developed progressive extrapyramidal symptoms that included blepharospasm, grimacing, and rigidity associated with increased iron deposition in the brain and visceral organs. Treatment for 10 months with the iron chelator desferrioxamine decreased brain iron stores, prevented progression of the neurological symptoms, and reduced plasma lipid peroxidation. These data suggest that early treatment with this chelator may be useful in such patients to diminish central nervous system iron accumulation and to prevent or ameliorate neurological symptoms associated with neurodegeneration.

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