Hematological profile of sickle cell disease in central India
نویسندگان
چکیده
منابع مشابه
Hematological profile of sickle cell disease from South Gujarat, India
The aim of this study was to determine hematological profile of sickle cell disease (SCD) from Surat, South Gujarat, India. This prospective cross-sectional study was conducted in the Department of Pediatrics and Sickle Cell Anemia Laboratory, Faculty of Pathology, Government Medical College, Surat, India, between July 2009 and December 2010. Patients included in this study were in their steady...
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Patients registered/enrolled in sickle cell clinic at NSCB Medical College Jabalpur were studied to understand the clinical profile and natural history of sickle cell disease (SCD) and also to evolve standard guidelines for management and prevention of the disease. Splenomegaly was reported in 67.7% patients. Non-palpable spleen was observed in 30.3 % patients. The most frequent clinical sympto...
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330 clinically suspected sickle cell disease (SCD) patients admitted to Dept. of Pediatrics, Medical College & Hospital, Raipur (Chhattisgarh) between 9 months to 14 years of age within the time period of May 2000 to September 2007 were chosen as subjects for this study. The diagnosis of SCD was confirmed by Sodium Metabisulphite method. On the basis of the results of electrophoresis the subjec...
متن کاملSickle cell disease in India.
A screening programme involving 9,822 hospitalised patients revealed the frequency of individuals with S gene to be 11.1 per cent. A population survey of 1,000 randomised subjects from amongst about 70,000 people in one block of the area showed the frequency to be 15.1%. The gene is not confined to tribal peoples, but is prevalent throughout the society, being more frequent in scheduled castes ...
متن کاملIntracardiac Thrombosis in Sickle Cell Disease
In patients with sickle cell disease, thrombotic microangiopathy is a rare complication. Also in sickle cell disease, intracardiac thrombus formation without structural heart diseases or atrial arrhythmias is a rare phenomenon. We herein describe a 22-year-old woman, who was a known case of sickle cell-βthalassemia, had a history of recent missed abortion, and was admitted with a vaso-occlusive...
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ژورنال
عنوان ژورنال: Indian Journal of Hematology and Blood Transfusion
سال: 2007
ISSN: 0971-4502,0974-0449
DOI: 10.1007/s12288-008-0005-z