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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: 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 …
Surgical correction of Hallermann-Streiff syndrome: a case report of esotropia, entropion, and blepharoptosis.
Cho WK, Park JW, Park MR. Cho WK, et al. Korean J Ophthalmol. 2011 Apr;25(2):142-5. doi: 10.3341/kjo.2011.25.2.142. Epub 2011 Mar 14. Korean J Ophthalmol. 2011. PMID: 21461230 Free PMC article.
We report a case of surgical treatment for Hallermann-Streiff syndrome in a patient with ocular manifestations of esotropia, entropion, and blepharoptosis. ...
We report a case of surgical treatment for Hallermann-Streiff syndrome in a patient with ocular manifestations of esotr …
Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?
Spaepen A, Schrander-Stumpel C, Fryns JP, de Die-Smulders C, Borghgraef M, Van den Berghe H. Spaepen A, et al. Am J Med Genet. 1991 Dec 15;41(4):517-20. doi: 10.1002/ajmg.1320410428. Am J Med Genet. 1991. PMID: 1663704
We describe 3 young children with Hallermann-Streiff syndrome, 2 with typical manifestations and 1 with the facial changes without the eye abnormalities but with a cleft palate and with complete syndactyly of fingers IV and V. The latter case represents overl …
We describe 3 young children with Hallermann-Streiff syndrome, 2 with typical manifestations and 1 with the facial chan …
Livebirth prevalence and follow-up of malformation syndromes in 27,472 newborns.
Higurashi M, Oda M, Iijima K, Iijima S, Takeshita T, Watanabe N, Yoneyama K. Higurashi M, et al. Brain Dev. 1990;12(6):770-3. doi: 10.1016/s0387-7604(12)80004-0. Brain Dev. 1990. PMID: 2092586
There were 29 cases with trisomy-21; 5 cases with trisomy-13 syndrome; 5 with trisomy-18 syndrome; 2 with cri-du-chat syndrome; and one each with partial monosomy 4p, partial trisomy 5p, partial trisomy 6p, partial trisomy 9p, partial trisomy 9q, partial monosomy 10p, and partial …
There were 29 cases with trisomy-21; 5 cases with trisomy-13 syndrome; 5 with trisomy-18 syndrome; 2 with cri-du-chat syndrome; and one each …
Cardiorespiratory disease associated with Hallermann-Streiff syndrome: analysis of craniofacial morphology by cephalometric roentgenograms.
Friede H, Lopata M, Fisher E, Rosenthal IM. Friede H, et al. J Craniofac Genet Dev Biol Suppl. 1985;1:189-98. J Craniofac Genet Dev Biol Suppl. 1985. PMID: 3877095
This paper analyzes the craniofacial morphology in a patient with typical Hallermann-Streiff syndrome (HSS) who developed symptomatic cardiorespiratory deficiency at the age of 48 years. ...
This paper analyzes the craniofacial morphology in a patient with typical Hallermann-Streiff syndrome (HSS) who develop …
A typical Hallermann-Streiff syndrome in a 3 year old child.
Vadiakas G, Oulis C, Tsianos E, Mavridou S. Vadiakas G, et al. J Clin Pediatr Dent. 1995 Fall;20(1):63-8. J Clin Pediatr Dent. 1995. PMID: 8634201 Review.
Hallermann Streiff syndrome is a rare congenital disorder characterized by dyscephaly, dental anomalies, proportionate nanism, hypotrichosis, cutaneous atrophy limited to the head, bilateral congenital cataracts and bilateral microphthalmia. ...
Hallermann Streiff syndrome is a rare congenital disorder characterized by dyscephaly, dental anomalies, proportionate …
MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication.
Fryns JP, Borghgraef M, Lemmens F, van den Berghe H. Fryns JP, et al. Clin Genet. 1993 Sep;44(3):146-8. doi: 10.1111/j.1399-0004.1993.tb03866.x. Clin Genet. 1993. PMID: 8275573
The clinical symptoms and signs observed in this child up to the age of 14 months were most compatible with the diagnosis of Hallermann-Streiff syndrome....
The clinical symptoms and signs observed in this child up to the age of 14 months were most compatible with the diagnosis of Hallermann …
Evaluation and surgical correction of the facial skeletal deformity in Hallermann-Streiff syndrome.
Sclaroff A, Eppley BL. Sclaroff A, et al. Int J Oral Maxillofac Surg. 1987 Dec;16(6):738-44. doi: 10.1016/s0901-5027(87)80061-9. Int J Oral Maxillofac Surg. 1987. PMID: 3125273
A case of Hallermann-Streiff syndrome (HSS) is presented. The syndrome characteristics and differential diagnoses are reviewed. ...
A case of Hallermann-Streiff syndrome (HSS) is presented. The syndrome characteristics and differential diagnoses are r …
Review of cases presenting with microcephaly and bilateral congenital cataract in a paediatric cataract clinic.
Goyal R, Thompson D, Timms C, Wilson LC, Russell-Eggitt I. Goyal R, et al. Eye (Lond). 2008 Feb;22(2):273-81. doi: 10.1038/sj.eye.6702958. Epub 2007 Nov 2. Eye (Lond). 2008. PMID: 17975563
RESULTS: In our series, three children were diagnosed with early-onset Cockayne syndrome (CS2), one was diagnosed with Micro syndrome and one with Hallermann-Streiff syndrome. Electrodiagnostic testing was abnormal in four of the five cases, and growth failur …
RESULTS: In our series, three children were diagnosed with early-onset Cockayne syndrome (CS2), one was diagnosed with Micro syndrome and on …
11 results