Beta Thalassemia and Klinefelter syndrome: a rare occurrence
Abstract Background β-Thalassemia is an inherited haematological blood disorder in the HBB gene, and variations in this HBB gene lead to the absence/deficiency of the Beta chain synthesis of haemoglobin leading to severe anaemia. Klinefelter syndrome is a chromosomal abnormality that affects physica...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
SpringerOpen
2022-05-01
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Series: | Egyptian Journal of Medical Human Genetics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s43042-022-00300-1 |