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Pearson's syndrome (medical condition): Pearson's anemia is a rare progressive condition characterized by abnormal pancreatic functioning and sideroblastic anemia. Diagnosis usually occurs within the first 7 years of life and death in infancy is common.
See also:
Pearson's anemia:
»Introduction: Pearson's anemia
»Symptoms of Pearson's anemia
»Treatments for Pearson's anemia
These medical condition or symptom topics may be relevant to medical information for Pearson's syndrome:
Pearson's syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pearson's syndrome, or a subtype of Pearson's syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Pearson's syndrome: Another name for Pearson's anemia (or close medical condition association).
»Introduction: Pearson's anemia
»Symptoms of Pearson's anemia
»Treatments for Pearson's anemia
Some of the symptoms of Pearson's syndrome incude:
See full list of 20 symptoms of Pearson's syndrome (Pearson's anemia)
Treatments for Pearson's syndrome (Pearson's anemia) include:
Read more about treatments for Pearson's syndrome
Treatment of Pearson's syndrome: For more treatment information about Pearson's syndrome, see treatment of Pearson's anemia (Pearson's syndrome)
Source - NIH
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