Von Willebrand disease historical perspective: Difference between revisions
Jump to navigation
Jump to search
Prince Djan (talk | contribs) |
Iqra Qamar (talk | contribs) |
||
| (5 intermediate revisions by 3 users not shown) | |||
| Line 2: | Line 2: | ||
{{Von Willebrand disease}} | {{Von Willebrand disease}} | ||
{{CMG}} | {{CMG}} {{AE}} {{PTD}} {{N.F}} | ||
==Overview== | ==Overview== | ||
[[Von Willebrand's disease]] was first described by [[Erik Adolf von Willebrand]], a Finnish [[paediatrics|pediatrician]] in 1926. Dr. [[Erik Adolf von Willebrand]] was also the first to differentiate [[Von Willebrand's disease]] from [[hemophilia]]. [[Von Willebrand's disease]] was initially named [[hereditary]] pseudo hemophilia. In the mid 1950s it was recognized that [[Von Willebrand's disease]] was usually accompanied by decreased level of coagulation [[factor VIII]] (FVIII) activity. In the early 1970s the immunologic distinction between [[FVIII]] and [[von Willebrand factor]] was established. In the 1980s, cloning of the VWF gene was investigated which has facilitated investigation into the genetic basis of VWD. | |||
==Historical Perspective== | ==Historical Perspective== | ||
*[[Von Willebrand's disease]] was first described by [[Erik Adolf von Willebrand]], a Finnish [[paediatrics|paediatrician]] in 1926.<ref>{{WhoNamedIt|doctor|2690}}</ref><ref name="pmid23020315">{{cite journal| author=Lenting PJ, Casari C, Christophe OD, Denis CV| title=von Willebrand factor: the old, the new and the unknown. | journal=J Thromb Haemost | year= 2012 | volume= 10 | issue= 12 | pages= 2428-37 | pmid=23020315 | doi=10.1111/jth.12008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23020315 }} </ref> | *[[Von Willebrand's disease]] was first described by [[Erik Adolf von Willebrand]], a Finnish [[paediatrics|paediatrician]] in 1926.<ref>{{WhoNamedIt|doctor|2690}}</ref><ref name="pmid23020315">{{cite journal| author=Lenting PJ, Casari C, Christophe OD, Denis CV| title=von Willebrand factor: the old, the new and the unknown. | journal=J Thromb Haemost | year= 2012 | volume= 10 | issue= 12 | pages= 2428-37 | pmid=23020315 | doi=10.1111/jth.12008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23020315 }} </ref> | ||
*Dr. [[Erik Adolf von Willebrand]] was also the first to | *Dr. [[Erik Adolf von Willebrand]] was also the first to differentiate [[Von Willebrand's disease]] from hemophilia.<ref name="pmid23020315">{{cite journal| author=Lenting PJ, Casari C, Christophe OD, Denis CV| title=von Willebrand factor: the old, the new and the unknown. | journal=J Thromb Haemost | year= 2012 | volume= 10 | issue= 12 | pages= 2428-37 | pmid=23020315 | doi=10.1111/jth.12008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23020315 }} </ref> | ||
*[[Von Willebrand's disease]] was initially named hereditary | *[[Von Willebrand's disease]] was initially named hereditary pseudo hemophilia.<ref name="pmid23020315">{{cite journal| author=Lenting PJ, Casari C, Christophe OD, Denis CV| title=von Willebrand factor: the old, the new and the unknown. | journal=J Thromb Haemost | year= 2012 | volume= 10 | issue= 12 | pages= 2428-37 | pmid=23020315 | doi=10.1111/jth.12008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23020315 }} </ref> | ||
*In the mid 1950s it was recognized that [[Von Willebrand's disease]] was usually accompanied by the following:<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref> | *In the mid 1950s it was recognized that [[Von Willebrand's disease]] was usually accompanied by the following:<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref> | ||
**A decreased level of coagulation [[factor VIII]] (FVIII) activity | **A decreased level of coagulation [[factor VIII]] (FVIII) activity | ||
**Bleeding phenotype could be corrected by the infusion of normal plasma. | **Bleeding phenotype could be corrected by the infusion of normal [[plasma]]. | ||
*In the early 1970s the immunologic distinction between [[FVIII]] and [[von Willebrand factor]] was made.<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref> | *In the early 1970s the immunologic distinction between [[FVIII]] and [[von Willebrand factor]] was made.<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref> | ||
*In the 1980s, cloning of the VWF gene was investigated which has facilitated investigation into the genetic basis of VWD.<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref><ref name="pmid3873280">{{cite journal| author=Lynch DC, Zimmerman TS, Collins CJ, Brown M, Morin MJ, Ling EH et al.| title=Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method. | journal=Cell | year= 1985 | volume= 41 | issue= 1 | pages= 49-56 | pmid=3873280 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3873280 }} </ref><ref name="pmid2864688">{{cite journal| author=Sadler JE, Shelton-Inloes BB, Sorace JM, Harlan JM, Titani K, Davie EW| title=Cloning and characterization of two cDNAs coding for human von Willebrand factor. | journal=Proc Natl Acad Sci U S A | year= 1985 | volume= 82 | issue= 19 | pages= 6394-8 | pmid=2864688 | doi= | pmc=390722 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2864688 }} </ref><ref name="pmid3874428">{{cite journal| author=Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA et al.| title=Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. | journal=Science | year= 1985 | volume= 228 | issue= 4706 | pages= 1401-6 | pmid=3874428 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3874428 }} </ref><ref name="pmid3019665">{{cite journal| author=Verweij CL, Diergaarde PJ, Hart M, Pannekoek H| title=Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit. | journal=EMBO J | year= 1986 | volume= 5 | issue= 8 | pages= 1839-47 | pmid=3019665 | doi= | pmc=1167049 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3019665 }} </ref> | *In the 1980s, cloning of the VWF gene was investigated which has facilitated investigation into the [[genetic]] basis of VWD.<ref name="pmid21289515">{{cite journal| author=James PD, Goodeve AC| title=von Willebrand disease. | journal=Genet Med | year= 2011 | volume= 13 | issue= 5 | pages= 365-76 | pmid=21289515 | doi=10.1097/GIM.0b013e3182035931 | pmc=3832952 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21289515 }} </ref><ref name="pmid3873280">{{cite journal| author=Lynch DC, Zimmerman TS, Collins CJ, Brown M, Morin MJ, Ling EH et al.| title=Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method. | journal=Cell | year= 1985 | volume= 41 | issue= 1 | pages= 49-56 | pmid=3873280 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3873280 }} </ref><ref name="pmid2864688">{{cite journal| author=Sadler JE, Shelton-Inloes BB, Sorace JM, Harlan JM, Titani K, Davie EW| title=Cloning and characterization of two cDNAs coding for human von Willebrand factor. | journal=Proc Natl Acad Sci U S A | year= 1985 | volume= 82 | issue= 19 | pages= 6394-8 | pmid=2864688 | doi= | pmc=390722 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2864688 }} </ref><ref name="pmid3874428">{{cite journal| author=Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA et al.| title=Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. | journal=Science | year= 1985 | volume= 228 | issue= 4706 | pages= 1401-6 | pmid=3874428 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3874428 }} </ref><ref name="pmid3019665">{{cite journal| author=Verweij CL, Diergaarde PJ, Hart M, Pannekoek H| title=Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit. | journal=EMBO J | year= 1986 | volume= 5 | issue= 8 | pages= 1839-47 | pmid=3019665 | doi= | pmc=1167049 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3019665 }} </ref> | ||
==References== | ==References== | ||
Latest revision as of 14:03, 12 September 2018
|
Von Willebrand disease Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Von Willebrand disease historical perspective On the Web |
|
American Roentgen Ray Society Images of Von Willebrand disease historical perspective |
|
Risk calculators and risk factors for Von Willebrand disease historical perspective |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Prince Tano Djan, BSc, MBChB [2] Nazia Fuad M.D.
Overview
Von Willebrand's disease was first described by Erik Adolf von Willebrand, a Finnish pediatrician in 1926. Dr. Erik Adolf von Willebrand was also the first to differentiate Von Willebrand's disease from hemophilia. Von Willebrand's disease was initially named hereditary pseudo hemophilia. In the mid 1950s it was recognized that Von Willebrand's disease was usually accompanied by decreased level of coagulation factor VIII (FVIII) activity. In the early 1970s the immunologic distinction between FVIII and von Willebrand factor was established. In the 1980s, cloning of the VWF gene was investigated which has facilitated investigation into the genetic basis of VWD.
Historical Perspective
- Von Willebrand's disease was first described by Erik Adolf von Willebrand, a Finnish paediatrician in 1926.[1][2]
- Dr. Erik Adolf von Willebrand was also the first to differentiate Von Willebrand's disease from hemophilia.[2]
- Von Willebrand's disease was initially named hereditary pseudo hemophilia.[2]
- In the mid 1950s it was recognized that Von Willebrand's disease was usually accompanied by the following:[3]
- A decreased level of coagulation factor VIII (FVIII) activity
- Bleeding phenotype could be corrected by the infusion of normal plasma.
- In the early 1970s the immunologic distinction between FVIII and von Willebrand factor was made.[3]
- In the 1980s, cloning of the VWF gene was investigated which has facilitated investigation into the genetic basis of VWD.[3][4][5][6][7]
References
- ↑ Template:WhoNamedIt
- ↑ 2.0 2.1 2.2 Lenting PJ, Casari C, Christophe OD, Denis CV (2012). "von Willebrand factor: the old, the new and the unknown". J Thromb Haemost. 10 (12): 2428–37. doi:10.1111/jth.12008. PMID 23020315.
- ↑ 3.0 3.1 3.2 James PD, Goodeve AC (2011). "von Willebrand disease". Genet Med. 13 (5): 365–76. doi:10.1097/GIM.0b013e3182035931. PMC 3832952. PMID 21289515.
- ↑ Lynch DC, Zimmerman TS, Collins CJ, Brown M, Morin MJ, Ling EH; et al. (1985). "Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method". Cell. 41 (1): 49–56. PMID 3873280.
- ↑ Sadler JE, Shelton-Inloes BB, Sorace JM, Harlan JM, Titani K, Davie EW (1985). "Cloning and characterization of two cDNAs coding for human von Willebrand factor". Proc Natl Acad Sci U S A. 82 (19): 6394–8. PMC 390722. PMID 2864688.
- ↑ Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA; et al. (1985). "Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization". Science. 228 (4706): 1401–6. PMID 3874428.
- ↑ Verweij CL, Diergaarde PJ, Hart M, Pannekoek H (1986). "Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit". EMBO J. 5 (8): 1839–47. PMC 1167049. PMID 3019665.