Hereditary spherocytosis laboratory findings: Difference between revisions
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* In a [[peripheral blood smear]], the abnormally small [[red blood cell]]s lacking the central pallor as seen in [[spherocytosis|non-hereditary spherocytosis]] is typically more marked in hereditary spherocytosis. | * In a [[peripheral blood smear]], the abnormally small [[red blood cell]]s lacking the central pallor as seen in [[spherocytosis|non-hereditary spherocytosis]] is typically more marked in hereditary spherocytosis. | ||
* [[Reticulocytosis]] | * [[Reticulocytosis]] | ||
* Decreased | * Decreased [[mean corpuscular volume]] | ||
* Increased | * Increased [[mean corpuscular hemoglobin concentration]] | ||
* Increased [[red cell distribution width]] | |||
==References== | ==References== | ||
Revision as of 18:35, 24 September 2012
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Hereditary spherocytosis Microchapters |
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Differentiating Hereditary spherocytosis from other Diseases |
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Hereditary spherocytosis laboratory findings On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Laboratory Findings
- In a peripheral blood smear, the abnormally small red blood cells lacking the central pallor as seen in non-hereditary spherocytosis is typically more marked in hereditary spherocytosis.
- Reticulocytosis
- Decreased mean corpuscular volume
- Increased mean corpuscular hemoglobin concentration
- Increased red cell distribution width