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Acatalasemia Swiss type (medical condition): A rare inherited disorder involving a lack of erythrocyte catalase activity which affects lipid metabolism. The defect can manifest as one of two variants: Japanese variant (Takahara disease) or the Swiss variant which is asymptomatic.
See also:
Acatalasemia:
»Introduction: Acatalasemia
»Symptoms of Acatalasemia
»Treatments for Acatalasemia
These medical condition or symptom topics may be relevant to medical information for Acatalasemia Swiss type:
Acatalasemia Swiss type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acatalasemia Swiss type, or a subtype of Acatalasemia Swiss type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Acatalasemia Swiss type: Another name for Acatalasemia (or close medical condition association).
»Introduction: Acatalasemia
»Symptoms of Acatalasemia
»Treatments for Acatalasemia
Some of the symptoms of Acatalasemia Swiss type incude:
Read more about symptoms of Acatalasemia Swiss type (Acatalasemia)
Treatments for Acatalasemia Swiss type (Acatalasemia) include:
Read more about treatments for Acatalasemia Swiss type
Treatment of Acatalasemia Swiss type: For more treatment information about Acatalasemia Swiss type, see treatment of Acatalasemia (Acatalasemia Swiss type)
Source - NIH
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