Hereditary spherocytosis: Difference between revisions
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==Case Studies== | ==Case Studies== | ||
[[Hereditary spherocytosis case study one|Case #1]] | [[Hereditary spherocytosis case study one|Case #1]] | ||
==Related Chapters== | ==Related Chapters== |
Revision as of 17:30, 21 September 2012
Template:DiseaseDisorder infobox
Hereditary spherocytosis Microchapters |
Differentiating Hereditary spherocytosis from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Hereditary spherocytosis On the Web |
American Roentgen Ray Society Images of Hereditary spherocytosis |
Risk calculators and risk factors for Hereditary spherocytosis |
For patient information click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Historical Perspective
Classification
Pathophysiology
Differentiating Hereditary spherocytosis from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies