Document Detail


Development of hypogammaglobulinaemia in a patient with common variable immunodeficiency.
MedLine Citation:
PMID:  2612505     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A 3-year-old boy who developed common variable immunodeficiency was investigated for the development of hypogammaglobulinaemia. During a period of 4 years, the combined deficiency of IgA, IgG2 and IgG4 proceeded to include IgG1 and finally IgG3 and IgM. This order of isotypes of IgG subclass deficiencies corresponded to the gene order for the heavy chain constant region for immunoglobulins on chromosome 14.
Authors:
A Ishizaka; M Nakanishi; S Yamada; Y Sakiyama; S Matsumoto
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  European journal of pediatrics     Volume:  149     ISSN:  0340-6199     ISO Abbreviation:  Eur. J. Pediatr.     Publication Date:  1989 Dec 
Date Detail:
Created Date:  1990-03-12     Completed Date:  1990-03-12     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7603873     Medline TA:  Eur J Pediatr     Country:  GERMANY, WEST    
Other Details:
Languages:  eng     Pagination:  175-6     Citation Subset:  IM    
Affiliation:
Department of Paediatrics, Hokkaido University School of Medicine, Kitaku Sapporo, Japan.
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MeSH Terms
Descriptor/Qualifier:
Agammaglobulinemia / blood,  etiology*,  physiopathology
Child, Preschool
Humans
IgA Deficiency
IgG Deficiency
Immunoglobulin A / analysis
Immunoglobulin G / analysis
Immunoglobulin M / analysis,  deficiency
Immunologic Deficiency Syndromes / complications*
Male
Chemical
Reg. No./Substance:
0/Immunoglobulin A; 0/Immunoglobulin G; 0/Immunoglobulin M

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


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