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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1970 3
1980 1
1987 1
1990 1
1991 5
1993 2
1995 1
1996 1
1999 1
2001 1
2002 1
2003 2
2004 2
2007 2
2008 3
2009 2
2010 2
2011 3
2013 2
2014 1
2015 2
2016 1
2018 4
2019 1
2021 2
2022 1
2024 0

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46 results

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Page 1
Hallermann-Streiff syndrome.
Suzuki Y, Fujii T, Fukuyama Y. Suzuki Y, et al. Dev Med Child Neurol. 1970 Aug;12(4):496-506. doi: 10.1111/j.1469-8749.1970.tb01945.x. Dev Med Child Neurol. 1970. PMID: 5457544 No abstract available.
Diagnosis, Early Care, and Treatment of Hallermann-Streiff Syndrome: A Review of the Literature.
Godzieba A, Smektała T, Dowgierd K, Sporniak-Tutak K, Kowalski J. Godzieba A, et al. Pediatr Ann. 2021 May;50(5):e227-e231. doi: 10.3928/19382359-20210415-01. Epub 2021 May 1. Pediatr Ann. 2021. PMID: 34044702 Review.
Hallermann-Streiff syndrome is a rare congenital disorder characterized by a wide spectrum of craniofacial abnormalities. ...
Hallermann-Streiff syndrome is a rare congenital disorder characterized by a wide spectrum of craniofacial abnormalitie …
Hallermann-Streiff syndrome: a review.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet. 1991 Dec 15;41(4):488-99. doi: 10.1002/ajmg.1320410423. Am J Med Genet. 1991. PMID: 1776643 Review.
The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, micrognathia, and proportionate short stature. ...
The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, …
Hallermann-Streiff syndrome: A missing molecular link for a highly recognizable syndrome.
Schmidt J, Wollnik B. Schmidt J, et al. Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):398-406. doi: 10.1002/ajmg.c.31668. Am J Med Genet C Semin Med Genet. 2018. PMID: 30580479 Review.
The use of modern next-generation sequencing-based approaches for gene identification has tremendously improved our understanding of the molecular pathogenesis of the great majority of well-known syndromes, whereas only a few remain to be elucidated. Hallermann-Streiff …
The use of modern next-generation sequencing-based approaches for gene identification has tremendously improved our understanding of the mol …
Syndromes with supernumerary teeth.
Lubinsky M, Kantaputra PN. Lubinsky M, et al. Am J Med Genet A. 2016 Oct;170(10):2611-6. doi: 10.1002/ajmg.a.37763. Epub 2016 Jun 2. Am J Med Genet A. 2016. PMID: 27250821 Review.
An association of a Mendelian disorder with a low frequency manifestation of supernumerary teeth is difficult to exclude without large numbers, but several commonly cited syndromes lacked evidence for clear association, including Hallermann-Streiff syndrome, …
An association of a Mendelian disorder with a low frequency manifestation of supernumerary teeth is difficult to exclude without large numbe …
Hallermann-Streiff syndrome.
Neki AS. Neki AS. Indian J Ophthalmol. 1993 Jul;41(2):83-4. Indian J Ophthalmol. 1993. PMID: 8262609 Free article. No abstract available.
Hallermann Streiff syndrome: Cranio-facial manifestations systematic review and report of two cases.
Preudhomme R, Veyssiere A, Ambroise B, Benateau H. Preudhomme R, et al. J Stomatol Oral Maxillofac Surg. 2022 Sep;123(4):e219-e223. doi: 10.1016/j.jormas.2021.11.002. Epub 2021 Nov 17. J Stomatol Oral Maxillofac Surg. 2022. PMID: 34800747
Hallermann Streiff syndrome (HSS) is a rare congenital abnormality with about 200 case reports in the literature. ...
Hallermann Streiff syndrome (HSS) is a rare congenital abnormality with about 200 case reports in the literature. ...
Hallermann-Streiff syndrome: case report and literature review.
Robotta P, Schafer E. Robotta P, et al. Quintessence Int. 2011 Apr;42(4):331-8. Quintessence Int. 2011. PMID: 21516279 Review.
Hallermann-Streiff syndrome is a rare genetic disorder characterized primarily by head and face abnormalities. ...This article provides a case report of a 9-year-old boy with Hallermann-Streiff syndrome. Extraoral examination revealed a b …
Hallermann-Streiff syndrome is a rare genetic disorder characterized primarily by head and face abnormalities. ...This …
Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literature.
Christian CL, Lachman RS, Aylsworth AS, Fujimoto A, Gorlin RJ, Lipson MH, Graham JM Jr. Christian CL, et al. Am J Med Genet. 1991 Dec 15;41(4):508-14. doi: 10.1002/ajmg.1320410426. Am J Med Genet. 1991. PMID: 1776646 Review.
Hallermann-Streiff syndrome (HSS) is a rare disorder with an associated constellation of radiological findings that may aid in the diagnosis of affected individuals. ...
Hallermann-Streiff syndrome (HSS) is a rare disorder with an associated constellation of radiological findings that may …
Hallermann-Streiff syndrome: a case review.
Mirshekari A, Safar F. Mirshekari A, et al. Clin Exp Dermatol. 2004 Sep;29(5):477-9. doi: 10.1111/j.1365-2230.2004.01572.x. Clin Exp Dermatol. 2004. PMID: 15347328 Review.
Hallermann-Streiff Syndrome is a rare genetic disorder that is characterized primarily by head and face abnormalities. Patients show bird-like facies, dental abnormalities, and hypotrichosis with various ophthalmic abnormalities. We report here a 26-year-old …
Hallermann-Streiff Syndrome is a rare genetic disorder that is characterized primarily by head and face abnormalities. …
46 results