Progeria historical perspective: Difference between revisions
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===Discovery=== | ===Discovery=== | ||
* Hutchinson-Gilford progeria syndrome or progeria was first discovered by DeBusk. | *[[Hutchinson-Gilford progeria syndrome]] or [[progeria]] was first discovered by DeBusk. | ||
*The name to the disease as progeria was given by Hastings Gilford. | *The name to the [[disease]] as [[progeria]] was given by Hastings Gilford. | ||
*Jonathan Hutchinson previously menton the disease progeria disorder and written about progeria. | *Jonathan Hutchinson previously menton the disease [[progeria]] disorder and written about [[progeria]]. | ||
*Paterson reported 2 cases of progeria in 2 brothers who parents had consanguineous marriage. | *Paterson reported 2 cases of [[progeria]] in 2 brothers who parents had [[consanguineous]] marriage. | ||
*In 1986, Ogihara et al reported a case in japan who might have progeria and survived till 45 years which is unusually long life span for the disease. | *In 1986, Ogihara et al reported a case in japan who might have [[progeria]] and survived till 45 years which is unusually long life span for the disease. | ||
*In 1987, Dyck et al reported a patient who had progeria and underwent | *In 1987, Dyck et al reported a patient who had [[progeria]] and underwent [[coronary artery bypass surgery]] and [[percutaneous]] [[Transluminal percutaneous coronary angioplasty|transluminal]] [[angioplasty]]. | ||
*In 1987, De Martinville et al reported 3 cases of neonatal Hutchinson-Gilford progeria syndrome in france. | *In 1987, De Martinville et al reported 3 cases of [[neonatal]] [[Hutchinson-Gilford progeria syndrome]] in france. | ||
*In 1990, Parkash et al noticed mandibuloacral dysplasia in a patient who is suffering with progeria. | *In 1990, Parkash et al noticed mandibuloacral [[dysplasia]] in a patient who is suffering with [[progeria]]. | ||
*In 1990, Fatunde et al reported progeria in 3 out of 6 siblings in a family. | *In 1990, Fatunde et al reported [[progeria]] in 3 out of 6 siblings in a family. | ||
*In 2002, De Paula Rodrigues et al described the involvement of bones and joints in progeria patients. | *In 2002, De Paula Rodrigues et al described the involvement of [[Bone (disambiguation)|bones]] and [[Joint|joints]] in [[progeria]] patients. | ||
*In 2006, Hennekam described the phenotypes of Hutchinson-Gilford progeria syndrome. | *In 2006, Hennekam described the [[Phenotype|phenotypes]] of [[Hutchinson-Gilford progeria syndrome]]. | ||
*In 2008, Merideth et al studied 15 patients who are suffering with Hutchinson-Gilford progeria syndrome very comprehensively | *In 2008, Merideth et al studied 15 patients who are suffering with [[Hutchinson-Gilford progeria syndrome|Hutchinson-Gilford progeria syndrom]]<nowiki/>e very comprehensively about the features of the [[disease]] and well documented. | ||
===Landmark Events in the Development of Treatment Strategies=== | ===Landmark Events in the Development of Treatment Strategies=== | ||
Revision as of 16:09, 2 July 2019
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Progeria Microchapters |
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Progeria historical perspective On the Web |
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Risk calculators and risk factors for Progeria historical perspective |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Historical Perspective
Discovery
- Hutchinson-Gilford progeria syndrome or progeria was first discovered by DeBusk.
- The name to the disease as progeria was given by Hastings Gilford.
- Jonathan Hutchinson previously menton the disease progeria disorder and written about progeria.
- Paterson reported 2 cases of progeria in 2 brothers who parents had consanguineous marriage.
- In 1986, Ogihara et al reported a case in japan who might have progeria and survived till 45 years which is unusually long life span for the disease.
- In 1987, Dyck et al reported a patient who had progeria and underwent coronary artery bypass surgery and percutaneous transluminal angioplasty.
- In 1987, De Martinville et al reported 3 cases of neonatal Hutchinson-Gilford progeria syndrome in france.
- In 1990, Parkash et al noticed mandibuloacral dysplasia in a patient who is suffering with progeria.
- In 1990, Fatunde et al reported progeria in 3 out of 6 siblings in a family.
- In 2002, De Paula Rodrigues et al described the involvement of bones and joints in progeria patients.
- In 2006, Hennekam described the phenotypes of Hutchinson-Gilford progeria syndrome.
- In 2008, Merideth et al studied 15 patients who are suffering with Hutchinson-Gilford progeria syndrome very comprehensively about the features of the disease and well documented.
Landmark Events in the Development of Treatment Strategies
Impact on Cultural History
Famous Cases
The following are a few famous cases of [disease name]: