| Literature DB >> 12712065 |
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.Entities:
Mesh:
Year: 2003 PMID: 12712065 DOI: 10.1067/mpd.2003.148
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406