Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 10204856.
- Also identified by PMC identifier 1734313.
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Abstract
A mother and daughter are reported with bilateral optic atrophy with onset in infancy and unilateral facial palsy. This appears to be a novel autosomal dominant disorder.
Medical subject headings
- Facial Paralysis
- Genes, Dominant
- Optic Atrophy