Alport syndrome: Difference between revisions
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''This article incorporates public domain text from [http://ghr.nlm.nih.gov The U.S. National Library of Medicine]'' | ''This article incorporates public domain text from [http://ghr.nlm.nih.gov The U.S. National Library of Medicine]'' | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Kidney diseases]] | [[Category:Kidney diseases]] |
Latest revision as of 13:49, 2 December 2016
For patient information on this page, click here Template:DiseaseDisorder infobox
Alport syndrome Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Alport syndrome On the Web |
American Roentgen Ray Society Images of Alport syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]
Synonyms and keywords: Hereditary nephritis; hemorrhagic familial nephritis; X-linked nephropathy and deafness; hematuria-nephropathy-deafness; hereditary deafness and nephropathy
Overview
Historical Perspective
Pathophysiology
Causes
Differentiating Alport syndrome from other Diseases
Epidemiology and Demographics
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Criteria | History and Symptoms | Physical Examination | Laboratory Findings | Echocardiography or Ultrasound | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
This article incorporates public domain text from The U.S. National Library of Medicine