A new form of autosomal dominant arthrogryposis.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1941966.
- Also identified by PMC identifier 1017058.
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Abstract
We report a man and his son with congenital limb contractures, limitation of ocular movements, and an electroretinal abnormality. They appear to have an autosomal dominant form of arthrogryposis, distinguishable from other previously classified forms of this disorder.
Medical subject headings
- Arthrogryposis
- Genes, Dominant