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{{Microangiopathic hemolytic anemia}} | {{Microangiopathic hemolytic anemia}} | ||
The “[[microangiopathic hemolytic anemia]]” term was first coined by Symmers, a British [[physician]] in 1952. He described 33 [[patient]]s presenting with constellation of symptoms of varying severity. The symptoms included [[fever]], [[hemolytic anemia]], [[thrombocytopenia]] and [[neurological]] deterioration<ref name="pmid12978378">{{cite journal| author=SYMMERS WS| title=Thrombotic microangiopathic haemolytic anaemia (thrombotic microangiopathy). | journal=Br Med J | year= 1952 | volume= 2 | issue= 4790 | pages= 897-903 | pmid=12978378 | doi=10.1136/bmj.2.4790.897 | pmc=2021829 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12978378 }} </ref>. The [[neurological]] symptoms usually present at the latter course of the [[disease]]. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} |
Latest revision as of 13:55, 26 January 2021
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The “microangiopathic hemolytic anemia” term was first coined by Symmers, a British physician in 1952. He described 33 patients presenting with constellation of symptoms of varying severity. The symptoms included fever, hemolytic anemia, thrombocytopenia and neurological deterioration[1]. The neurological symptoms usually present at the latter course of the disease.
References
- ↑ SYMMERS WS (1952). "Thrombotic microangiopathic haemolytic anaemia (thrombotic microangiopathy)". Br Med J. 2 (4790): 897–903. doi:10.1136/bmj.2.4790.897. PMC 2021829. PMID 12978378.