Hereditary spherocytosis differential diagnosis: Difference between revisions
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==Overview== | ==Overview== | ||
==Differential diagnosis== | ==Differential diagnosis== | ||
* Glucose-6-phosphate dehydrogenase deficiency | * [[Glucose-6-phosphate dehydrogenase deficiency]] | ||
* Hemoglobin H disease | * [[Hemoglobin H disease]] | ||
* Autoimmune hemolytic | * [[Autoimmune hemolytic anemia]]s or [[alloimmune hemolytic anemia]] (eg, [[ABO incompatibility]]) | ||
* Extrinsic nonimmune hemolytic anemia due to systemic disease | * Extrinsic nonimmune hemolytic anemia due to systemic disease | ||
* Microangiopathic hemolytic anemia | * [[Microangiopathic hemolytic anemia]] | ||
==References== | ==References== | ||
Revision as of 18:51, 24 September 2012
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Hereditary spherocytosis Microchapters |
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Differentiating Hereditary spherocytosis from other Diseases |
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Diagnosis |
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Treatment |
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Hereditary spherocytosis differential diagnosis On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Differential diagnosis
- Glucose-6-phosphate dehydrogenase deficiency
- Hemoglobin H disease
- Autoimmune hemolytic anemias or alloimmune hemolytic anemia (eg, ABO incompatibility)
- Extrinsic nonimmune hemolytic anemia due to systemic disease
- Microangiopathic hemolytic anemia