Document Detail


Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.
MedLine Citation:
PMID:  21274562     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION: Clinical manifestations and immunoglobulin levels of the patients with Hyper-IgM type 4 phenotype recovered in late childhood at about 6 years of age. There was a transient CSR defect which was not observed in cases with transient hypogammaglobulinemia of infancy. Detection of a non-AID or non-UNG associated CSR defect in infancy should be confirmed later on since spontaneous recovery may occur.
Authors:
Neslihan Edeer Karaca; Anne Durandy; Nesrin Gulez; Guzide Aksu; Necil Kutukculer
Publication Detail:
Type:  Journal Article; Review     Date:  2011-01-28
Journal Detail:
Title:  European journal of pediatrics     Volume:  170     ISSN:  1432-1076     ISO Abbreviation:  Eur. J. Pediatr.     Publication Date:  2011 Aug 
Date Detail:
Created Date:  2011-07-19     Completed Date:  2012-03-16     Revised Date:  2014-07-30    
Medline Journal Info:
Nlm Unique ID:  7603873     Medline TA:  Eur J Pediatr     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  1039-47     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
B-Lymphocyte Subsets / metabolism
Child
Child, Preschool
Female
Follow-Up Studies
Humans
Hyper-IgM Immunodeficiency Syndrome / complications,  genetics,  immunology*
Immunoglobulins / blood*
Lymphocyte Count
Male
Phenotype
Remission, Spontaneous
Retrospective Studies
Chemical
Reg. No./Substance:
0/Immunoglobulins

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


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