Papillorenal syndrome: Difference between revisions
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==Case Studies== | ==Case Studies== | ||
[[Papillorenal syndrome case study one|Case #1]] | [[Papillorenal syndrome case study one|Case #1]] | ||
{{Congenital malformations of genital organs and urinary system}} | {{Congenital malformations of genital organs and urinary system}} | ||
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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
[[Category:Disease]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} |
Revision as of 13:40, 28 September 2012
Papillorenal syndrome | |
OMIM | 120330 |
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DiseasesDB | 32086 |
Papillorenal syndrome Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Papillorenal syndrome On the Web |
American Roentgen Ray Society Images of Papillorenal syndrome |
For patient information click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords:: Renal-coloboma syndrome; isolated renal hypoplasia
Overview
Historical Perspective
Pathophysiology
Differentiating Papillorenal syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Laboratory Findings | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies