Document Detail


Bronchial mucous glands in the newborn with cystic fibrosis.
MedLine Citation:
PMID:  7182186     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The size of bronchial mucous glands in 21 patients who presented with meconium ileus and died at less than three weeks of age were compared quantitatively with that of 28 control patients. There were no significant differences by most methods of comparison. However, pulmonary infection was seen in a higher percentage of cystic fibrosis patients. The absence of mucous gland hyperplasia at birth suggests that mucous obstruction of airways may not be primarily responsible for the increased susceptibility to respiratory tract infection in cystic fibrosis, but when present later in life may aggravate the infection.
Authors:
C W Chow; L I Landau; L M Taussig
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  European journal of pediatrics     Volume:  139     ISSN:  0340-6199     ISO Abbreviation:  Eur. J. Pediatr.     Publication Date:  1982 Dec 
Date Detail:
Created Date:  1983-07-08     Completed Date:  1983-07-08     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7603873     Medline TA:  Eur J Pediatr     Country:  GERMANY, WEST    
Other Details:
Languages:  eng     Pagination:  240-3     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Bronchi / pathology*,  secretion
Cystic Fibrosis / complications*,  pathology
Female
Humans
Infant, Newborn
Intestine, Small / pathology
Male
Mucus / secretion
Respiratory Tract Infections / etiology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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