Four individuals in a single family affected with maxillofacial dysostosis are reported. Maxillary hypoplasia, delayed onset of speech, and poor development of language skills without associated hearing loss are the main characteristics of the syndrome which is transmitted as an autosomal dominant. Cephalometric analysis and speech and hearing evaluation of the patients confirmed the above findings.
|Original language||English (US)|
|Number of pages||4|
|Journal||Journal of Medical Genetics|
|State||Published - Dec 1 1977|
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