Literature DB >> 12712065

Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome.

Martin Frühwirth1, Andreas R Janecke, Thomas Müller, Victoria E H Carlton, Florian Kronenberg, Felix Offner, A S Knisely, Silvana Geleff, Eyun J Song, Burkhard Simma, Alfred Königsrainer, Raimund Margreiter, C B van der Hagen, Kristin Eiklid, Oystein Aagenaes, Laura Bull, Helmut Ellemunter.   

Abstract

Lymphedema-cholestasis syndrome (LCS, Aagenaes syndrome) is the only known form of hereditary lymphedema associated with cholestasis. A locus, LCS1, has recently been mapped to chromosome 15q in a Norwegian kindred. In a consanguine Serbian Romani family with a neonate who had a combination of lymphedema and cholestasis with features atypical for Norwegian LCS, haplotype and linkage analysis of markers spanning the LCS1 region argue that a second LCS locus may exist. The infant may represent an instance of a previously undescribed lymphedema-cholestasis syndrome.

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Year:  2003        PMID: 12712065     DOI: 10.1067/mpd.2003.148

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  5 in total

1.  The nuclear hormone receptor Coup-TFII is required for the initiation and early maintenance of Prox1 expression in lymphatic endothelial cells.

Authors:  R Sathish Srinivasan; Xin Geng; Ying Yang; Yingdi Wang; Suraj Mukatira; Michèle Studer; Marianna P R Porto; Oleg Lagutin; Guillermo Oliver
Journal:  Genes Dev       Date:  2010-04-01       Impact factor: 11.361

Review 2.  Genetics of familial intrahepatic cholestasis syndromes.

Authors:  S W C van Mil; R H J Houwen; L W J Klomp
Journal:  J Med Genet       Date:  2005-06       Impact factor: 6.318

3.  Angioid streaks in aagenaes syndrome.

Authors:  Viara Shoumnalieva-Ivanova; Ivan Tanev; Yani Zdravkov; Simeon Monov; Russka Shumnalieva
Journal:  Int Ophthalmol       Date:  2016-09-10       Impact factor: 2.031

4.  Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.

Authors:  Sajid Malik; Karl-Heinz Grzeschik
Journal:  Hum Genet       Date:  2008-01-10       Impact factor: 4.132

5.  CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops.

Authors:  Sohela Shah; Laura K Conlin; Luis Gomez; Øystein Aagenaes; Kristin Eiklid; A S Knisely; Michael T Mennuti; Randolph P Matthews; Nancy B Spinner; Laura N Bull
Journal:  PLoS One       Date:  2013-09-26       Impact factor: 3.240

  5 in total

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