VASO-OCCLUSIVE CRISIS IN A PATIENT WITH SICKLE CELL TRAIT

VASO-OCCLUSIVE CRISIS IN A PATIENT WITH SICKLE CELL TRAIT

Sickle cell trait occurs as a result of inheritance of a normal haemoglobin gene (HbA) from one parent and a mutated sickle haemoglobin (HbS) gene from another. Unlike the sickle cell disease, it is considered a benign condition in itself. However, major vaso-occlusive complications have been report...

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Veröffentlicht in:Journal of Chitwan Medical College 2023-12, Vol.13 (4), p.111-113
Hauptverfasser: Neupane, Pradeep, Ranjan, Mukesh Kumar, Yadav, Roshan Kumar, Timalsina, Ekanta
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container_issue 4
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container_title Journal of Chitwan Medical College
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creator Neupane, Pradeep
Ranjan, Mukesh Kumar
Yadav, Roshan Kumar
Timalsina, Ekanta
description Sickle cell trait occurs as a result of inheritance of a normal haemoglobin gene (HbA) from one parent and a mutated sickle haemoglobin (HbS) gene from another. Unlike the sickle cell disease, it is considered a benign condition in itself. However, major vaso-occlusive complications have been reported in association with Sickle cell trait, the acute chest syndrome being the most important one. We report the case details of a 32 years male who presented with features of acute chest syndrome and was later found to have sickle cell trait.  
doi_str_mv 10.54530/jcmc.1359
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