Case Reports
The Nagar syndrome (acrofacial dysostosis): evidence for autosomal dominant inheritance
- PMID: 890111
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Case Reports
The Nagar syndrome (acrofacial dysostosis): evidence for autosomal dominant inheritance
Birth Defects Orig Artic Ser.
1977.
Abstract
A 10-year-old girl with the Nagar acrofacial dysostosis syndrome and normal intelligence is presented. Severe conductive hearing loss remains the major handicap. It is suggested that her syndrome is due to a dominant gene mutation.
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