Case Reports
doi: 10.1136/jmg.14.5.355.
Maxillofacial dysostosis
- PMID: 592352
- PMCID: PMC1013620
- DOI: 10.1136/jmg.14.5.355
Item in Clipboard
Case Reports
Maxillofacial dysostosis
J Med Genet.
1977 Oct.
Abstract
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 our patients confirmed the above findings.
Similar articles
-
A new autosomal dominant acrofacial dysostosis syndrome.Am J Med Genet Suppl. 1986;2:143-50. doi: 10.1002/ajmg.1320250618. Am J Med Genet Suppl. 1986. PMID: 3146284 Review.
-
Autosomal dominant Goldenhar syndrome.Birth Defects Orig Artic Ser. 1982;18(6):621-8. Birth Defects Orig Artic Ser. 1982. PMID: 7171780 No abstract available.
-
Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia.Clin Genet. 1982 Mar;21(3):161-7. doi: 10.1111/j.1399-0004.1982.tb00957.x. Clin Genet. 1982. PMID: 7094392 No abstract available.
-
The Nagar syndrome (acrofacial dysostosis): evidence for autosomal dominant inheritance.Birth Defects Orig Artic Ser. 1977;13(3C):195-202. Birth Defects Orig Artic Ser. 1977. PMID: 890111
-
Penetrance and variability of major malformation syndromes associated with deafness.Birth Defects Orig Artic Ser. 1979;15(5B):207-26. Birth Defects Orig Artic Ser. 1979. PMID: 393321 Review. No abstract available.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
