Hereditary spherocytosis: Difference between revisions
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== [[hereditary spherocytosis laboratory findings|Laboratory Findings]] == | == [[hereditary spherocytosis laboratory findings|Laboratory Findings]] == | ||
== [[hereditary spherocytosis chest x ray|Chest X ray]] == | |||
== [[hereditary spherocytosis CT|CT]] == | |||
== [[hereditary spherocytosis MRI|MRI]] == | |||
== [[hereditary spherocytosis echocardiography or ultrasound| Echocardiography or Ultrasound]] == | |||
== [[hereditary spherocytosis other imaging findings|Other Imaging Findings]] == | |||
== [[hereditary spherocytosis other diagnostic studies|Other Diagnostic Studies]] == | |||
== [[hereditary spherocytosis medical therapy|Treatment]] == | == [[hereditary spherocytosis medical therapy|Treatment]] == | ||
Revision as of 17:16, 28 November 2018
Template:DiseaseDisorder infobox
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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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Case Studies |
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Hereditary spherocytosis On the Web |
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American Roentgen Ray Society Images of Hereditary spherocytosis |
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Risk calculators and risk factors for Hereditary spherocytosis |
For patient information click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Zahir Ali Shaikh, MD[2]
Overview
Hereditary spherocytosis is a genetically-transmitted form of spherocytosis, an auto-hemolytic anemia characterized by the production of red blood cells that are sphere-shaped rather than donut-shaped, and therefore more prone to hemolysis.