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J Pediatr ; 142(4): 441-7, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12712065

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.


Subject(s)
Cholestasis/complications , Cholestasis/genetics , Genetic Heterogeneity , Lymphedema/complications , Lymphedema/genetics , Cholestasis/congenital , Chromosome Mapping , Genetic Linkage/genetics , Haplotypes/genetics , Humans , Infant, Newborn , Lymphedema/congenital , Male , Pedigree , Syndrome
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