Document Detail


Infantile alpha 1 antitrypsin deficiency: a case report.
MedLine Citation:
PMID:  7727562     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Using a case study format, the authors describe an infant with an unusual metabolic disorder, Alpha 1 Antitrypsin Deficiency. It is rare to find an infant in whom such significant liver and pulmonary disease develops before his first birthday. In this article the authors describe the pathophysiology, genetics, diagnosis, and treatment of this disorder. The nursing diagnoses alteration in nutrition, alteration in skin integrity, ineffective airway clearance, and potential for ineffective family coping are the framework used to describe the nursing care.
Authors:
C F Tinstman; J Crimlisk
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Gastroenterology nursing : the official journal of the Society of Gastroenterology Nurses and Associates     Volume:  18     ISSN:  1042-895X     ISO Abbreviation:  Gastroenterol Nurs     Publication Date:    1995 Jan-Feb
Date Detail:
Created Date:  1995-06-01     Completed Date:  1995-06-01     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8915377     Medline TA:  Gastroenterol Nurs     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  20-6     Citation Subset:  N    
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MeSH Terms
Descriptor/Qualifier:
Genetic Diseases, Inborn / diagnosis,  nursing*
Humans
Infant, Newborn
Male
Nursing Diagnosis
alpha 1-Antitrypsin Deficiency*

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


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