Approximately 150 cases have been reported in the literature worldwide.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:The purpose was to report a case of Hallermann-Streiff syndrome (HSS) with atypical presentation and present a brief literature review.
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Temel Bulgular & Veri:Hallermann in 1948 and Streiff in 1950 described patients characterized by "bird face," congenital cataract, mandibular hypoplasia, and dental abnormalities.
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Sonuç & Katkı:Approximately 150 cases have been reported in the literature worldwide.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri
Abstract
The purpose was to report a case of Hallermann-Streiff syndrome (HSS) with atypical presentation and present a brief literature review. Hallermann in 1948 and Streiff in 1950 described patients characterized by "bird face," congenital cataract, mandibular hypoplasia, and dental abnormalities. The new syndrome was later defined as HSS, underlining the differences with regard to Franceschetti's mandibulofacial dysostosis. HSS is associated with developmental anomalies involving structures of ectodermal origin (the face, scull, hair, skin, eyes, and teeth) and overall growth and development. Approximately 150 cases have been reported in the literature worldwide.
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Bu Makaleye Atıf Yap
BHADANE, P., JOSHİ, S., AHİRAAO, M. (2016). Hallermann-Streiff Syndrome--Confluence of Systems. Erciyes Medical Journal, Cilt: 38 - Sayı: 1, 43–45. https://ajindex.com/articles/223512
Tuna EB, Sulun T, Rosti O, Abdallah FE, Kayserili H, Aktoren O. Cra- niodentofacial manifestations in Hallermann Streiff syndrome. Cranio The Journal of Craniomandibular Practice, Jan 2009.
MC Lee, Im CJ, Jin JW. A Case Hallermann-Streiff Syndrome with aphakia. Korean Journal of Pediatrics 2008; 51(6): 646-9. [CrossRef] Francois J. A new syndrome; dyscephalia with bird face and dental anomalies, nanism, hypotrichosis, cutaneous atrophy, microphthal- mia, and congenital cataract. Arch Ophthalmol 1958; 60(5): 842-62. [CrossRef] Dennis NR, Fairhurst J, Moore IE. Lethal syndrome of slender bones, intrauterine fractures, characteristics facial appearance, and cataracts, resembling Hallermann-Streiff syndrome in two sibs. Am J Med Genet 1995; 59(4): 517-20. [CrossRef] Gerinec A. The hallermann-Streiff syndrome in two generations. Ces- tofthalmol 1989; 45: 326-33.
Schanzlin DJ, Goldberg DB, Brown SI. Hallermann-Streiff Syndrome associated with sclerocornea, aniridia and chromosomal abnormality. Am J Ophthalmol 1980; 9(3): 411-5. [CrossRef] Cohen MM Jr. Hallermann-Streiff syndrome: a review. Am J Med Genet 1991; 41(4): 488-99. [CrossRef] http://www.healthline.com/galecontent/hallerman-streiff- syndrome/5#ixzz1DLLD344DU Mirshekari A, Safar F. Hallermann-Streiff syndrome: A case review. Clin Exp Dermatol 2004; 29(5): 477-9. [CrossRef] David LR, Finlon M, Genecov D, Argenta LC. Hallermann-Streiff syndrome: Experience with 15 patients and review of the literature. J Craniofac Surg 1999; 10: 160-8. [CrossRef]