This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 1970 Jun;7(2):185-8.

doi: 10.1136/jmg.7.2.185.

Hemifacial microsomia--oculo-auriculo-vertebral dysplasia. A patient with overlapping features

H Pashayan, L Pinsky, F C Fraser

PMID: 4997787
PMCID: PMC1468807
DOI: 10.1136/jmg.7.2.185

Hemifacial microsomia--oculo-auriculo-vertebral dysplasia. A patient with overlapping features

H Pashayan et al. J Med Genet. 1970 Jun.

. 1970 Jun;7(2):185-8.

doi: 10.1136/jmg.7.2.185.

Authors

H Pashayan, L Pinsky, F C Fraser

PMID: 4997787
PMCID: PMC1468807
DOI: 10.1136/jmg.7.2.185

No abstract available

PubMed Disclaimer

Similar articles

The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B, Balikova I, Bradinova I, Zahariev D, Popova A, Simeonov E, De Smet L, Devriendt K, Fryns JP. Dimitrov B, et al. Genet Couns. 2005;16(2):181-6. Genet Couns. 2005. PMID: 16080300 No abstract available.
[The oculo-oto-vertebral syndrome (author's transl)].
Müller WD, Stern E. Müller WD, et al. Klin Padiatr. 1977 Nov;189(6):417-22. Klin Padiatr. 1977. PMID: 414017 German.
Rubinstein-Taybi syndrome.
Berry AC. Berry AC. J Med Genet. 1987 Sep;24(9):562-6. doi: 10.1136/jmg.24.9.562. J Med Genet. 1987. PMID: 3312608 Free PMC article. Review. No abstract available.
Mandibulofacial dysostosis or bilateral hemifacial microsomia with hearing loss, telecanthus, tetramelic postaxial hexadactyly, congenital hypotonia and lymphedema with joint hypermobility, and pigmentary dysplasia: a new syndrome?
Opitz JM, Reynolds JF, FitzGerald JM. Opitz JM, et al. Am J Med Genet. 1989 Aug;33(4):433-5. doi: 10.1002/ajmg.1320330402. Am J Med Genet. 1989. PMID: 2556918 No abstract available.
Clinical and radiographic variations in hemifacial microsomia.
Coccaro PJ, Becker MH, Converse JM. Coccaro PJ, et al. Birth Defects Orig Artic Ser. 1975;11(2):314-24. Birth Defects Orig Artic Ser. 1975. PMID: 776245 Review.

See all similar articles

Cited by

Clinical and cytogenetic features of a Brazilian sample of patients with phenotype of oculo-auriculo-vertebral spectrum: a cross-sectional study.
Silva AP, Rosa RF, Trevisan P, Dorneles JC, Mesquita CS, Mattos VF, Paskulin GA, Zen PR. Silva AP, et al. Sao Paulo Med J. 2015 May-Jun;133(3):191-8. doi: 10.1590/1516-3180.2013.7762204. Epub 2014 Oct 17. Sao Paulo Med J. 2015. PMID: 25337663 Free PMC article.
Long-standing chin-augmenting costochondral graft creating a diagnostic challenge: A case report and literature review.
Badr FF, Mintline M, Ruprecht A, Cohen D, Blumberg BR, Nair MK. Badr FF, et al. Imaging Sci Dent. 2016 Dec;46(4):279-284. doi: 10.5624/isd.2016.46.4.279. Epub 2016 Dec 20. Imaging Sci Dent. 2016. PMID: 28035307 Free PMC article.
Goldenhar syndrome and hemifacial microsomia: observations on three patients.
Thomas P. Thomas P. Eur J Pediatr. 1980 May;133(3):287-92. doi: 10.1007/BF00496092. Eur J Pediatr. 1980. PMID: 7389743
Sleep outcomes in children with hemifacial microsomia and controls: a follow-up study.
Cloonan YK, Kifle Y, Davis S, Speltz ML, Werler MM, Starr JR. Cloonan YK, et al. Pediatrics. 2009 Aug;124(2):e313-21. doi: 10.1542/peds.2008-3488. Epub 2009 Jul 27. Pediatrics. 2009. PMID: 19651569 Free PMC article.

References

1. Am J Ophthalmol. 1966 Oct;62(4):678-82 - PubMed
1. Br Med J. 1968 Feb 24;1(5590):489-90 - PubMed
1. Ann Ocul (Paris). 1953 Feb;186(2):155-69 - PubMed
1. J Genet Hum. 1958 Oct;7(3):143-73 - PubMed
1. J Pediatr. 1963 Nov;63:991-9 - PubMed

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources