Detection of Hb variants and hemoglobinopathies in Indian population using HPLC: Report of 2600 cases
Author(s) -
Ritesh Sachdev,
ArpitaR Dam,
Gaurav Tyagi
Publication year - 2010
Publication title -
indian journal of pathology and microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.217
H-Index - 31
eISSN - 0974-5130
pISSN - 0377-4929
DOI - 10.4103/0377-4929.59185
Subject(s) - hemoglobin , hemoglobin variants , thalassemia , hemoglobinopathy , beta thalassemia , medicine , hemoglobin c , population , hemoglobin s , hemoglobin e , abnormality , gastroenterology , hemolytic anemia , disease , environmental health , sickle cell anemia , psychiatry
Inherited abnormalities of hemoglobin synthesis include a myriad of disorders ranging from thalassemia syndromes to structurally abnormal hemoglobin variants. Identification of these disorders is immensely important epidemiologically and aid in prevention of more serious hemoglobin disorders.
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