Hereditary elliptocytosis historical perspective: Difference between revisions
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==Overview== | ==Overview== | ||
==Historical Perspective== | ==Historical Perspective== | ||
RBC anomaly in [[Hereditary elliptocytosis]] was first observed in 1860 by Goltz,<ref name=":0">{{Cite web|url=https://jcp.bmj.com/content/jclinpath/14/6/615.full.pdf|title=Hereditary elliptocytic anaemia|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref> | |||
and Elliptocytosis, elliptical shape of RBCs was described in 1904 by Dresbach.<ref name="pmid17730874">{{cite journal| author=Dresbach M| title=ELLIPTICAL HUMAN RED CORPUSCLES. | journal=Science | year= 1904 | volume= 19 | issue= 481 | pages= 469-70 | pmid=17730874 | doi=10.1126/science.19.481.469 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17730874 }}</ref>Bishop recognized the familial inheritance as autosomal dominant of HE in 1914 and Hunter and Adams affirmed it's hereditary condition in 1929. <ref name=":0" /> Recent studies demonstrate that, the severity of symptoms in patients with Hereditary elliptocytosis is variable and it can be related to genetic variations. <ref name="pmid10027705.">{{cite journal| author=Tse WT, Lux SE| title=Red blood cell membrane disorders. | journal=Br J Haematol | year= 1999 | volume= 104 | issue= 1 | pages= 2-13 | pmid=10027705. | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10027705 }}</ref> | |||
==References== | ==References== | ||
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[[Category:Hematology]] | [[Category:Hematology]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
Revision as of 08:37, 12 August 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Historical Perspective
RBC anomaly in Hereditary elliptocytosis was first observed in 1860 by Goltz,[1]
and Elliptocytosis, elliptical shape of RBCs was described in 1904 by Dresbach.[2]Bishop recognized the familial inheritance as autosomal dominant of HE in 1914 and Hunter and Adams affirmed it's hereditary condition in 1929. [1] Recent studies demonstrate that, the severity of symptoms in patients with Hereditary elliptocytosis is variable and it can be related to genetic variations. [3]
References
- ↑ 1.0 1.1 "Hereditary elliptocytic anaemia" (PDF).
- ↑ Dresbach M (1904). "ELLIPTICAL HUMAN RED CORPUSCLES". Science. 19 (481): 469–70. doi:10.1126/science.19.481.469. PMID 17730874.
- ↑ Tse WT, Lux SE (1999). "Red blood cell membrane disorders". Br J Haematol. 104 (1): 2–13. PMID 10027705. Check
|pmid=value (help).