Hereditary spherocytic hemolytic anemia
Hereditary spherocytic hemolytic anemia: Introduction
Hereditary spherocytic hemolytic anemia: An inherited blood disorder where a metabolic defect causes defects in the red blood cells membranes which leads to their characteristic spherical shape (normal cells are doughnut shaped) and premature destruction.
More detailed information about the symptoms,
causes, and treatments of Hereditary spherocytic hemolytic anemia is available below.
Symptoms of Hereditary spherocytic hemolytic anemia
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symptoms of Hereditary spherocytic hemolytic anemia
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Wrongly Diagnosed with Hereditary spherocytic hemolytic anemia?
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Causes of Hereditary spherocytic hemolytic anemia
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Medical Textbooks Online about Hereditary spherocytic hemolytic anemia
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Less Common Symptoms of Hereditary spherocytic hemolytic anemia
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occasional symptoms of Hereditary spherocytic hemolytic anemia
Hereditary spherocytic hemolytic anemia: Medical Mistakes
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Hereditary spherocytic hemolytic anemia: Undiagnosed Conditions
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Misdiagnosis and Hereditary spherocytic hemolytic anemia
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Hereditary spherocytic hemolytic anemia: Rare Types
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Definitions of Hereditary spherocytic hemolytic anemia:
Hereditary spherocytic hemolytic anemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hereditary spherocytic hemolytic anemia, or a subtype of Hereditary spherocytic hemolytic anemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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