Hereditary spherocytosis historical perspective: Difference between revisions
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==Overview== | ==Overview== | ||
The [[hereditary spherocytosis]] was first described in 1871 by Vanlair and Masius, where they described [[Chronic (medical)|chronically]] [[Jaundice|icteric]] [[Patient|patients]] who had no [[bile]] in the [[urine]], no evidence of [[Hepato-biliary diseases|liver disease]] and often [[splenomegaly]] and [[family history]] of [[jaundice]]. It is the commonest [[Causality|cause]] of [[inherited]] [[Chronic (medical)|chronic]] [[hemolysis]] in the northern europe and north america. | |||
==Historical Perspective== | ==Historical Perspective== | ||
* Hereditary spherocytosis was first described in 1871 by Vanlair and Masius, where they described chronically icteric patients who had no bile in the urine, no evidence of liver disease and often splenomegaly and family history of jaundice.<ref>{{Cite journal | * [[Hereditary spherocytosis]] was first described in 1871 by Vanlair and Masius, where they described [[Chronic (medical)|chronically]] [[Jaundice|icteric]] [[Patient|patients]] who had no [[bile]] in the [[urine]], no evidence of [[Hepato-biliary diseases|liver disease]] and often [[splenomegaly]] and [[family history]] of [[jaundice]].<ref>{{Cite journal | ||
| author = [[Sayeeda Huq]], [[Mark A. C. Pietroni]], [[Hafizur Rahman]] & [[Mohammad Tariqul Alam]] | | author = [[Sayeeda Huq]], [[Mark A. C. Pietroni]], [[Hafizur Rahman]] & [[Mohammad Tariqul Alam]] | ||
| title = Hereditary spherocytosis | | title = Hereditary spherocytosis | ||
| Line 20: | Line 20: | ||
| pmid = 20214092 | | pmid = 20214092 | ||
}}</ref> | }}</ref> | ||
* It is the commonest cause of inherited chronic hemolysis in the northern europe and north america.<ref>{{Cite journal | * It is the commonest [[Causality|cause]] of [[inherited]] [[Chronic (medical)|chronic]] [[hemolysis]] in the northern europe and north america.<ref>{{Cite journal | ||
| author = [[Sayeeda Huq]], [[Mark A. C. Pietroni]], [[Hafizur Rahman]] & [[Mohammad Tariqul Alam]] | | author = [[Sayeeda Huq]], [[Mark A. C. Pietroni]], [[Hafizur Rahman]] & [[Mohammad Tariqul Alam]] | ||
| title = Hereditary spherocytosis | | title = Hereditary spherocytosis | ||
| Line 31: | Line 31: | ||
| pmid = 20214092 | | pmid = 20214092 | ||
}}</ref> | }}</ref> | ||
* With remarkable discernment, Vanlair and Masius stated, ‘The [[jaundice]] of our patient appears to be a peculiar type of [[icterus]]. The fact that the patient’s mother and sister had a slight [[jaundice]] and that the sister had an [[enlarged spleen]] may indicate that this condition is one disease entity.'.<ref name="Packman2001">{{cite journal|last1=Packman|first1=Charles H.|title=The spherocytic Haemolytic Anaemias|journal=British Journal of Haematology|volume=112|issue=4|year=2001|pages=888–899|issn=0007-1048|doi=10.1046/j.1365-2141.2001.02440.x}}</ref> | * With remarkable discernment, Vanlair and Masius stated, ‘The [[jaundice]] of our [[patient]] appears to be a peculiar type of [[icterus]]. The fact that the patient’s mother and sister had a slight [[jaundice]] and that the sister had an [[enlarged spleen]] may indicate that this condition is one [[disease]] entity.'.<ref name="Packman2001">{{cite journal|last1=Packman|first1=Charles H.|title=The spherocytic Haemolytic Anaemias|journal=British Journal of Haematology|volume=112|issue=4|year=2001|pages=888–899|issn=0007-1048|doi=10.1046/j.1365-2141.2001.02440.x}}</ref> | ||
==References== | ==References== | ||
Latest revision as of 20:16, 2 December 2018
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Overview
The hereditary spherocytosis was first described in 1871 by Vanlair and Masius, where they described chronically icteric patients who had no bile in the urine, no evidence of liver disease and often splenomegaly and family history of jaundice. It is the commonest cause of inherited chronic hemolysis in the northern europe and north america.
Historical Perspective
- Hereditary spherocytosis was first described in 1871 by Vanlair and Masius, where they described chronically icteric patients who had no bile in the urine, no evidence of liver disease and often splenomegaly and family history of jaundice.[1]
- It is the commonest cause of inherited chronic hemolysis in the northern europe and north america.[2]
- With remarkable discernment, Vanlair and Masius stated, ‘The jaundice of our patient appears to be a peculiar type of icterus. The fact that the patient’s mother and sister had a slight jaundice and that the sister had an enlarged spleen may indicate that this condition is one disease entity.'.[3]
References
- ↑ Sayeeda Huq, Mark A. C. Pietroni, Hafizur Rahman & Mohammad Tariqul Alam (2010). "Hereditary spherocytosis". Journal of health, population, and nutrition. 28 (1): 107–109. PMID 20214092. Unknown parameter
|month=ignored (help) - ↑ Sayeeda Huq, Mark A. C. Pietroni, Hafizur Rahman & Mohammad Tariqul Alam (2010). "Hereditary spherocytosis". Journal of health, population, and nutrition. 28 (1): 107–109. PMID 20214092. Unknown parameter
|month=ignored (help) - ↑ Packman, Charles H. (2001). "The spherocytic Haemolytic Anaemias". British Journal of Haematology. 112 (4): 888–899. doi:10.1046/j.1365-2141.2001.02440.x. ISSN 0007-1048.