Farara, Nashaat Elsayed (2015) Sickle Cell Thalassemia: A Case Report and Review of Literature. International Journal of Medical and Pharmaceutical Case Reports, 5 (5). pp. 1-4. ISSN 2394109X
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Abstract
Sickle cell disease is a single gene disorder causing a debilitating systemic syndrome characterized by chronic anaemia, acute painful episodes, organ infarction and chronic organ damage and by a significant reduction in life expectancy. Combined sickle cell beta thalassemia disease is the most common form of sickle cell disease in people of Mediterranean descent, including people of Italian, Greek or Turkish heritage. We experienced a three years old girl who was admitted with bronchopneumonia and found to have anaemia which was proved to be sickle cell thalassemia.
Conclusion: Sickle cell disease should be considered in pneumonic child with severe anemia.
Item Type: | Article |
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Subjects: | East India Archive > Medical Science |
Depositing User: | Unnamed user with email support@eastindiaarchive.com |
Date Deposited: | 04 Jul 2023 04:37 |
Last Modified: | 07 Jun 2024 10:53 |
URI: | http://ebooks.keeplibrary.com/id/eprint/1337 |