Hypoplastic Bone Marrow Failure in a Patient with Hereditary Persistence of Foetal Haemoglobin (HPFH) Trait
Hereditary Persistence of Foetal Haemoglobin (HPFH) trait is a rare genetic disorder and is caused by a large deletion involving δ and β globin genes. It is characterised by persistence of Foetal Haemoglobin (HbF) even in an adult. HbF level may vary from 2 to 30% in carriers of HPFH. Clinically, HP...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Private Limited
2020-03-01
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| Series: | Journal of Clinical and Diagnostic Research |
| Subjects: | |
| Online Access: | https://jcdr.net/articles/PDF/13546/43368_F(KM)_CE[Ra1]_(SL)_PF1(AG_SHU)_PN(SL).pdf |