Microangiopathic hemolytic anemia classification: Difference between revisions
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{{Microangiopathic hemolytic anemia}} | {{Microangiopathic hemolytic anemia}} {{MSJ}} | ||
[[Microangiopathic hemolytic anemia] may be classified into primary subtype based on the [[genetic]] mutations and no known underlying [[disease]] and secondary subtype due to known underlying cause. | |||
* Primary: | |||
** [[Thrombotic thrombocytopenic purpura]] | |||
*** [[Congenital]] | |||
*** [[Acquired]] | |||
** [[Hemolytic Uremic Syndrome]] | |||
*** Shiga [[toxin]] [[E-coli]] | |||
*** Atypical | |||
*Secondary: | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 22:30, 21 January 2021
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Microangiopathic hemolytic anemia Microchapters |
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Differentiating Microangiopathic hemolytic anemia from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Microangiopathic hemolytic anemia classification On the Web |
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American Roentgen Ray Society Images of Microangiopathic hemolytic anemia classification |
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Microangiopathic hemolytic anemia classification in the news |
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Directions to Hospitals Treating Microangiopathic hemolytic anemia |
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Risk calculators and risk factors for Microangiopathic hemolytic anemia classification |
[[Microangiopathic hemolytic anemia] may be classified into primary subtype based on the genetic mutations and no known underlying disease and secondary subtype due to known underlying cause.
- Primary:
- Secondary: