You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 30 No. 2, February 1974 TABLE OF CONTENTS
  Archives
  •  Online Features
  ARTICLES
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Studies in Batten Disease

I. Peroxidase Deficiency in Granulocytes

Donald Armstrong, MS; Sandra Dimmitt, MS; Dale E. VanWormer, MD

Arch Neurol. 1974;30(2):144-152.


Abstract

Lipopigments are prominent in Batten disease (Batten-Spielmeyer-Vogt [BSV] syndrome) and are considered to represent end products of lipid peroxidation.

Peroxidase is an enzyme that can hydrolyze peroxides (hydrogen peroxide) and by this means reduce lipid peroxidation. Myeloperoxidase activity was markedly deficient in the white blood cells of four patients with the late infantile and juvenile forms of BSV. Deficient peroxidase activity was found by both histochemical and spectrophotometric methods using two different substrates (benzidine and phenylenediamine).

Other laboratory criteria, such as hypergranulation of the neutrophils, correlated with the peroxidase deficiency. Vacuolated lymphocytes were only useful inthe juvenile form.

The distinctive accumulation of ceroid in neurons and other cells of patients with this syndrome is attributable to deficient peroxidase activity. A short, fundamentally simple test for peroxidase activity in peripheral leukocytes is reported, and its usefulness illustrated.



Author Affiliations

Tulsa, Okla

From the Clinical Research Center, Hillcrest Medical Center, Tulsa, Okla.


Footnotes

Accepted for publication July 12, 1973.

Reprint requests to Clinical Research Center, Hillcrest Medical Center, 1120 S Utica, Tulsa, OK 74104 (Mr. Armstrong).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Topical Review: The Neuronal Ceroid-Lipofuscinoses
Goebel
J Child Neurol 1995;10:424-437.
ABSTRACT  

Identification of retinoyl complexes as the autofluorescent component of the neuronal storage material in Batten disease
Wolfe et al.
Science 1977;195:1360-1362.
ABSTRACT  

Skin Punch Biopsy in the Diagnosis of Juvenile Neuronal Ceroid-Lipofuscinosis: A Comparison With Leukocyte Peroxidase Assay
Farrell and Sumi
Arch Neurol 1977;34:39-44.
ABSTRACT  

Leukocyte Peroxidase Deficiency in a Family with a Dominant Form of Kuf's Disease
Armstrong et al.
Science 1974;186:155-156.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1974 American Medical Association. All Rights Reserved.