Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence
Haemoglobinopathies are the commonest haemolytic disorders, prevalent in India and form a major bulk of patients in most of the haematology outpatient clinics. β-thalassaemia is the commonest inherited haemolytic anaemia and presence of β-Thalassaemia Trait (BTT) goes mostly undetected due to its as...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Private Limited
2018-01-01
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| Series: | Journal of Clinical and Diagnostic Research |
| Subjects: | |
| Online Access: | https://jcdr.net/articles/PDF/11072/31302_230118_31302_CE(RA1)_F(T)_PF1(PG_GG)_PFA(VJ_AP)PFA(MJ_AnG)_PN(AP).pdf |
| Summary: | Haemoglobinopathies are the commonest haemolytic disorders, prevalent in India and form a major bulk of patients in most of the haematology outpatient clinics. β-thalassaemia is the commonest inherited haemolytic anaemia and presence of β-Thalassaemia Trait (BTT) goes mostly undetected due to its asymptomatic clinical course. However, BTT should be diagnosed so as to conduct a genetic counselling and to prevent the number of births of affected children in turn reducing the financial burden on the affected family. Detection of combined haemolytic anaemia is on a rise due to better screening modalities in haemoglobinopathies. We hereby present two cases of combined BTT and Hereditary Spherocytosis (HS), and their clinical outcome. |
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| ISSN: | 2249-782X 0973-709X |