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Microangiopathic hemolytic anemia, congenital (medical condition): A rare blood condition where small blood clots form in blood vessels which reduces the number of blood platelets and results in kidney failure, neurological symptoms and anemia.
See also:
Thrombotic thrombocytopenic purpura, congenital:
»Introduction: Thrombotic thrombocytopenic purpura, congenital
»Symptoms of Thrombotic thrombocytopenic purpura, congenital
These medical condition or symptom topics may be relevant to medical information for Microangiopathic hemolytic anemia, congenital:
Microangiopathic hemolytic anemia, congenital is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Microangiopathic hemolytic anemia, congenital, or a subtype of Microangiopathic hemolytic anemia, congenital,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Microangiopathic hemolytic anemia, congenital: Another name for Thrombotic thrombocytopenic purpura, congenital (or close medical condition association).
»Introduction: Thrombotic thrombocytopenic purpura, congenital
»Symptoms of Thrombotic thrombocytopenic purpura, congenital
Some of the causes of Microangiopathic hemolytic anemia, congenital are included in the list below:
Some of the symptoms of Microangiopathic hemolytic anemia, congenital incude:
Source - NIH
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