Literature DB >> 9237505

Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndrome.

S Kurtoglu1, M Dundar, I K Hallaç, K Uzüm, Y Okumuş, T Oktem.   

Abstract

Larsen's syndrome is characterised by multiple joint dislocations, flat face and talipes equinovarus. There is an autosomal dominant form and also a more severe autosomal recessive form. Several types of polycystic kidney disease have been reported in children. In this report we present an infant with a severe form of Larsen's syndrome (thought to be lethal Larsen-like), infantile-type polycystic kidney disease, biliary dysgenesis and osteosclerosis.

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Year:  1997        PMID: 9237505     DOI: 10.1111/j.1399-0004.1997.tb02500.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  1 in total

1.  Larsen syndrome--lethal variety.

Authors:  M L Kulkarni; Zaheeruddin Mohammed; Preethi M Kulkarni
Journal:  Indian J Pediatr       Date:  2005-12       Impact factor: 1.967

  1 in total

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