A Rare Case of Late-onset Hemochromatosis Due to H63D Syndrome, a Diagnostic Challenge
H63D Syndrome (linked to a rarer H63D mutation in the HFE gene than the commoner C282Y mutation) despite causing mild iron overload can lead to significant morbidity than typical hemochromatosis. A 60-year-old, presented with Bell’s palsy, on further enquiry, had generalized pruritus, constipation,...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
The Kandy Society of Medicine
2024-12-01
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| Series: | Sri Lanka Journal of Medicine |
| Subjects: | |
| Online Access: | https://account.sljm.sljol.info/index.php/sljo-j-sljm2/article/view/553 |
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