Confirmation of linkage of Sjögren-Larsson syndrome to chromosome 17 in families of different ethnic origins.
AUTOR(ES)
Lacour, M
RESUMO
Linkage analysis in two consanguineous pedigrees of Pakistani and English origin and one further Indian family in which affected subjects have Sjögren-Larsson syndrome (SLS) showed linkage to chromosome 17. Linkage of SLS to D17S783 and D17S805 has been reported in Swedish pedigrees, but since those data were generated from a single ethnic group originating from a common ancestor, there remained the question of whether this disease is genetically heterogeneous. This report confirms the linkage in non-Swedish pedigrees and, therefore, provides evidence to support a single locus for SLS.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1051883Documentos Relacionados
- Sjögren-Larsson syndrome in two sibs with peripheral nerve involvement and bisalbuminaemia
- Estudo clinico-molecular e analise da textura epidermica de pacientes com sindrome de Sjogren-Larsson
- Características clínicas e neurorradiológicas típicas na síndrome de Sjögren-Larsson
- Lipofuscin and melanin content of the retinal pigment epithelium in a case of Sjögren-Larsson syndrome.
- Sjögren-Larsson syndrome. Impaired fatty alcohol oxidation in cultured fibroblasts due to deficient fatty alcohol:nicotinamide adenine dinucleotide oxidoreductase activity.