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PMID: 5908967 Published · ppublish English Journal Article

Chediak-Higashi syndrome: hereditary gigantism of cytoplasmic organelles.

Science (New York, N.Y.) ·Vol. 151 ·No. 3706 ·1966-01-07 ·Pages 81-3

Windhorst DB, Zelickson AS, Good RA

Abstract

In the Chediak-Higashi syndrome, an anomalous hypopigmentation is associated with large lysosomal granules in the blood leukocytes. Since the inheritance pattern is that of an autosomal recessive trait, we postulated a common mechanism for these two primary features of the disease. Electron microscopy of melanocytes revealed that the pigmentary anomaly is indeed based on giant melanosomes. Since both types of granules, leukocytic and melanosomal, are characterized by limiting membranes, Chediak-Higashi disease may be a genetic disease of membranes.

MeSH Terms
Child Cytoplasmic Granules Female Hair/pathology Humans Leukocytes/pathology Microscopy, Electron Pigmentation Disorders/genetics,pathology
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Windhorst D B
Zelickson A S
Good R A
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1966-01-07
Pages
81-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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