Document Detail

Clinico-haematological profile of HbE syndrome in adults and children.
MedLine Citation:
PMID:  14965869     Owner:  NLM     Status:  MEDLINE    
Haemoglobin E beta thalassemia (HbE beta thalassemia) has a remarkable variability in clinical expression ranging from a mild form of thalassemia intermedia to a transfusion dependent condition. An overlap between the mild variety of HbE beta thalassemia and homozygous HbE disease is common, however, differentiation is required for early institution of therapy and for predicting the later clinical course. Fifty cases of Hb E syndrome comprising of 43 cases of Hb E beta thalassemia and 7 cases of homozygous HbE disease were studied. Their clinico- haematological features and results of high performance liquid chromatography (HPLC) were analysed.
S Tyagi; H P Pati; V P Choudhry; R Saxena
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Hematology (Amsterdam, Netherlands)     Volume:  9     ISSN:  1024-5332     ISO Abbreviation:  Hematology     Publication Date:  2004 Feb 
Date Detail:
Created Date:  2004-02-17     Completed Date:  2004-08-05     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9708388     Medline TA:  Hematology     Country:  England    
Other Details:
Languages:  eng     Pagination:  57-60     Citation Subset:  IM    
Department of Haematology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi.
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MeSH Terms
Age of Onset
Hematologic Tests
Hemoglobin E*
Middle Aged
beta-Thalassemia / blood,  diagnosis*,  genetics
Reg. No./Substance:
9034-61-1/Hemoglobin E

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