Progeria historical perspective: Difference between revisions

	Progeria Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Progeria from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X-ray
Echocardiography and Ultrasound
CT scan
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Interventions
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Progeria historical perspective On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Progeria historical perspective All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Progeria historical perspective
CDC on Progeria historical perspective
Progeria historical perspective in the news
Blogs on Progeria historical perspective
Directions to Hospitals Treating Psoriasis
Risk calculators and risk factors for Progeria historical perspective

Revision as of 16:04, 2 July 2019

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

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.

@@ Line 19: / Line 19: @@
 *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
+*In 2002, De Paula Rodrigues et al described the involvement of bones and joints in progeria patients.
-*In [year], [scientist] was the first to discover the association between [risk factor] and the development of [disease name].
+*In 2006, Hennekam described the phenotypes of Hutchinson-Gilford progeria syndrome.
-*In [year], [gene] mutations were first implicated in the pathogenesis of [disease name].
+*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===