Abstract
DOUBLE HETEROZYGOUS HbS/HbD INCIDENTALLY DIAGNOSED DURING PREGNANCY -A CASE REPORT

Suman Kumari, Tarun Sharma*, Deepika and Anand Raj Kalla

ABSTRACT

Compound heterozygous for HbS/HbD results in severe hemolytic anemia and a clinical syndrome similar to that of sickle cell disease. Here we report a case of pregnancy with HbSD in 23 yrs old G2P1L1 residing at Nagour district in Rajasthan in rural community presented in antenatal OPD at 35 weeks of pregnancy with complains of bodyache, chest pain and fever for 2 days. On examination she had icterus, pallor and bilateral pitting edema. Her height was 160 cm. and weight were 52 kg. abdominal examination suggested live intrauterine gestation of 34 weeks. Spleen and liver was not palpable.

Keywords: HbS-hemoglobin S, HbD-hemoglobin D, HbSD variant, sickle cell disease.


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