Polycystic kidney disease natural history: Difference between revisions

Jump to navigation Jump to search
Aarti Narayan (talk | contribs)
No edit summary
Aarti Narayan (talk | contribs)
No edit summary
Line 7: Line 7:
*Symptoms of polycystic kidney disease begin in the third or fourth decade of life. However, the renal [[cyst]]s can be detected as early as childhood or in utero.
*Symptoms of polycystic kidney disease begin in the third or fourth decade of life. However, the renal [[cyst]]s can be detected as early as childhood or in utero.
*The [[cyst]]s gradually grow in size replacing most of the renal tissue, compromising its normal function.
*The [[cyst]]s gradually grow in size replacing most of the renal tissue, compromising its normal function.
*[[Creatinine]] begins to built up and eventually the patient goes into [[end stage renal disease]].
*[[Creatinine]] begins to built up and the patient eventually goes into [[end stage renal disease]].


==Complications==
==Complications==

Revision as of 16:22, 20 August 2012

Polycystic kidney disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Polycystic kidney disease from other Diseases

Epidemiology and Demographics

Risk Factor

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Future or Investigational Therapies

Case Studies

Case #1

Polycystic kidney disease natural history On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Polycystic kidney disease natural history

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Polycystic kidney disease natural history

CDC on Polycystic kidney disease natural history

Polycystic kidney disease natural history in the news

Blogs on Polycystic kidney disease natural history

Directions to Hospitals Treating Polycystic kidney disease

Risk calculators and risk factors for Polycystic kidney disease natural history

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]

Overview

Polycystic kidney disease is a multiorgan and progressive disorder characterized by formation of cysts in kidney and other organs like pancreas, liver and spleen.

Natural History

  • Symptoms of polycystic kidney disease begin in the third or fourth decade of life. However, the renal cysts can be detected as early as childhood or in utero.
  • The cysts gradually grow in size replacing most of the renal tissue, compromising its normal function.
  • Creatinine begins to built up and the patient eventually goes into end stage renal disease.

Complications

Prognosis

  • The disease gets worse slowly. Eventually it leads to end-stage chronic renal failure.
  • It is also associated with liver disease, including infection of liver cysts.
  • Medical treatment may relieve symptoms for many years.
  • People with PKD who do not have other diseases may be good candidates for a kidney transplant.

References

Template:WH Template:WS