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. 26 No. 1, January 1972 TABLE OF CONTENTS
  Archives
  •  Online Features
  ORIGINAL 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
 •Citing articles on Web of Science (77)
 •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?

Trichopoliodystrophy

II. Pathological Changes in Skeletal Muscle and Nervous System

Nitya R. Ghatak, MB, BS; Asao Hirano, MD; Tung P. Poon, MD; Joseph H. French, MD

Arch Neurol. 1972;26(1):60-72.


Abstract

A skeletal muscle biopsy and the nervous system of a 21-month-old male child who died of trichopoliodystrophy were studied by light and electron microscopy. The fine structural alterations in the muscle consisted of accumulation of glycogen, pronounced interfibrillar vacuolation, "hyaline degeneration," distortion of the tubular system, and disorganization of the mitochondria containing dense granules. In addition to atrophy of the brain with widespread neuronal loss and reduction of the white matter, the Purkinje cells of the cerebellum showed multiple, short, tapering cytoplasmic processes. The changes in the spinal cord consisted of neuronal loss in the Clarke's column and degeneration of the spinocerebellar tracts. Neuronal mitochondria in the postmortem material showed conglomeration and dense granules. The neuropathological changes in this disorder appear to be characteristic. The significance of the muscle changes, however, remains obscure.



Author Affiliations

Bronx, NY

From the Division of Neuropathology, Department of Pathology, and the departments of neurology and pediatrics, Montefiore Hospital and Medical Center, and the Department of Pathology, Albert Einstein College of Medicine, Bronx, NY.


Footnotes

Accepted for publication Aug 12, 1971.

Reprint requests to Montefiore Hospital and Medical Center, Bronx, NY 10467 (Dr. French).



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

Neuropathology of Occipital Horn Syndrome
Palmer and Percy
J Child Neurol 2001;16:764-766.
ABSTRACT  

Familial Poliodystrophy, Mitochondrial Myopathy, and Lactate Acidemia
Hart et al.
Arch Neurol 1977;34:180-185.
ABSTRACT  

Fine Structure of the Cerebellar Cortex in Menkes Kinky-Hair Disease: X-Chromosome-Linked Copper Malabsorption
Hirano et al.
Arch Neurol 1977;34:52-56.
ABSTRACT  

Giant Axonal Neuropathy: A Clinically and Morphologically Distinct Neurological Disease
Carpenter et al.
Arch Neurol 1974;31:312-316.
ABSTRACT  

Menkes Kinky-Hair Syndrome (Trichopoliodystrophy) Low Copper Levels in the Blood, Hair, and Urine
Singh and Bresnan
Arch Pediatr Adolesc Med 1973;125:572-578.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1972 American Medical Association. All Rights Reserved.