Literature DB >> 9841713

Ivemark's renal-hepatic-pancreatic dysplasia: analytic approach to a perinatal autopsy.

R W Bendon1.   

Abstract

A case of Ivemark's renal-hepatic dysplasia syndrome is presented. The findings are suggestive of a ductal obstructive process anatomically located at the junction of ducts with the parenchyma. The differential diagnosis includes Meckel syndrome, short rib polydactyly syndromes, and glutaric aciduria type 2. The molecular basis for this syndrome remains unknown.

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Year:  1999        PMID: 9841713     DOI: 10.1007/s100249900096

Source DB:  PubMed          Journal:  Pediatr Dev Pathol        ISSN: 1093-5266


  4 in total

1.  Failure to Thrive, Jaundice, and Polyuria in Early Infancy: Common Presentation with an Uncommon Lethal Etiology.

Authors:  Sonia Sharma
Journal:  J Pediatr Genet       Date:  2019-11-11

2.  Renal-hepatic-pancreatic dysplasia syndrome (Ivemark's syndrome).

Authors:  Mahesha Vankalakunti; Kirti Gupta; Nandita Kakkar; Ashim Das
Journal:  Diagn Pathol       Date:  2007-07-02       Impact factor: 2.644

Review 3.  Renal-hepatic-pancreatic dysplasia-1 with a novel NPHP3 genotype: a case report and review of the literature.

Authors:  Hui Zhu; Zhi-Hui Zhao; Shu-Yao Zhu; Fu Xiong; Li-Hong He; Yong Zhang; Jin Wang
Journal:  BMC Pediatr       Date:  2022-10-18       Impact factor: 2.567

4.  Immunohistochemical study of the phenotypic change of the mesenchymal cells during portal tract maturation in normal and fibrous (ductal plate malformation) fetal liver.

Authors:  Julien Villeneuve; Fanny Pelluard-Nehme; Chantal Combe; Dominique Carles; Christine Chaponnier; Jean Ripoche; Charles Balabaud; Paulette Bioulac-Sage; Sébastien Lepreux
Journal:  Comp Hepatol       Date:  2009-07-14
  4 in total

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