Document Detail


Clinico-haematological profile of HbE syndrome in adults and children.
MedLine Citation:
PMID:  14965869     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
S Tyagi; H P Pati; V P Choudhry; R Saxena
Related Documents :
19906159 - A review of long-term prophylaxis in the rare inherited coagulation factor deficiencies.
25186999 - Successful treatment of calciphylaxis with intravenous sodium thiosulfate in a nonuremi...
25148619 - Congenital isolated aplasia of lower lateral cartilage and reconstruction using dorsal ...
25437569 - Causes of uveitis in a tertiary center in chile: a cross-sectional retrospective review.
25437679 - Inflammatory myofibroblastic tumor of the small-bowel mesentery: a case report of nonsp...
2719349 - Sulfite sensitivity: relationship between sulfite plasma levels and bronchospasm: case ...
24041829 - Muscle-specific kinase antibody positive myaesthenia gravis and multiple sclerosis co-p...
25489719 - Intravitreal injection technique and monitoring: updated guidelines of an expert panel.
14700109 - Hypo-estrogenemia in retinal vasculopathy due to primary antiphospholipid antibody synd...
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    
Affiliation:
Department of Haematology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi. drseematyagi@hotmail.com
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Age of Onset
Female
Hematologic Tests
Hemoglobin E*
Heterozygote
Homozygote
Humans
Male
Middle Aged
Phenotype
beta-Thalassemia / blood,  diagnosis*,  genetics
Chemical
Reg. No./Substance:
9034-61-1/Hemoglobin E

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


Previous Document:  Th1/Th2 cells in patients with multiple myeloma.
Next Document:  Plasma levels of TNF-alpha in sickle cell patients receiving hydroxyurea.