Abstract
Systemic sclerosis (SSc) is a multisystem connective tissue disease characterised phenotypically by fibrosis and ischaemic atrophy. Its aetiology is most likely multifactorial. A genetic predisposition to the condition is suggested by reports of familial SSc (a positive family history is the strongest risk factor yet identified), by animal models, and by disease-association studies, in which researchers have examined a wide variety of genes including those involved in fibrosis, in vascular function and structure, and in autoimmunity - the relative rarity of SSc has precluded linkage studies, except in the Choctaw Indians. Recent advances in genetic methodologies should further our understanding of this complex disease process.
Original language | English |
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Pages (from-to) | 165-168 |
Number of pages | 3 |
Journal | Arthritis Research |
Volume | 4 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2002 |
Keywords
- Candidate genes
- Genetic epidemiology
- Scleroderma
- Systemic sclerosis