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Dysplasia of the kidneys, liver, and pancreas: Report of a variant of Ivemark's syndrome

  • Published:1979-03 Issue:2 Volume:10 Page:228-234
  • ISSN:0046-8177
  • Container-title:Human Pathology
  • language:en
  • Short-container-title:Human Pathology

Author:

Strayer David S.,Kissane John M.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference46 articles.

1. Pathogenesis of polycystic kidneys: historical survey;Osthanondh;Arch. Path.,1964

2. Familial dysplasia of kidneys, liver, and pancreas: a probably genetically determined syndrome;Ivemark;Acta Paediatr.,1959

3. Facial characteristics of infants with bilateral renal agenesis;Potter;Am. J. Obstet. Gynecol.,1946

4. Pathogenesis of polycystic kidneys: type I due to hyperplasia of interstitial portions of collecting tubules;Osthanondh;Arch. Path.,1964

5. Pathogenesis of polycystic kidneys: type 2 due to inhibition of ampullary activity;Osthanondh;Arch. Path.,1964

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1. Parenchymal GI Glands (Gallbladder, Biliary Tract, and Pancreas);Pathology of Childhood and Adolescence;2020

2. Founders of Pediatric Pathology: Margaret G. Smith and John M. Kissane;Pediatric and Developmental Pathology;2016-07

3. Pancreas: Anatomy and Structural Anomalies;Yamada' s Textbook of Gastroenterology;2015-11-27

4. Cysts and Congenital Biliary Abnormalities;Sherlock's Diseases of the Liver and Biliary System;2011-05-05

5. Nephronophthisis and Renal–Hepatic–Pancreatic Dysplasia of Ivemark;Fibrocystic Diseases of the Liver;2010
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