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Journals / Erciyes Tıp Dergisi / 2003 / Cilt: 25 - Sayı: 4

Ocular findings in a case with Hallermann-streiff syndrome

Hallermann streiff sendromlu bir olguda göz bulguları

Tamer GÜNEŞ
Hakkı DOĞAN
Berrin KARAMAN
Ayşe ÖNER
Mehmet KÖSE
Pages
208–210
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this repon the clinical characteristics of an 11 year old case were presented.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Abstract: Hallermannn-Streiff syndrome is a rare congenital syndrome.
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Key Findings & Data:This syndrome is usually sporadic' and characterized by a bird-like face, mandibular and maxillary hypoplasia, ocular and dental abnormalities, skin atrophy and short stature.
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Conclusion & Impact:In this repon the clinical characteristics of an 11 year old case were presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Abstract: Hallermannn-Streiff syndrome is a rare congenital syndrome. This syndrome is usually sporadic' and characterized by a bird-like face, mandibular and maxillary hypoplasia, ocular and dental abnormalities, skin atrophy and short stature. In this repon the clinical characteristics of an 11 year old case were presented.

Özet

Özet: Hallermann-Streiff sendromu oldukça nadir görülen bir konjenital sendromdur. Genelde sporadik olarak ortaya çıkan bu sendrom kuşa benzer yüz görünümü, mandibula ve maksilla hipoplazisi, göz ve diş anomalileri, deri atrofisi ve ufak vücut yapısı ile karakterizedir. Bu yazıda 11 yaşındaki bir olgunun klinik özellikleri sunulmuştur.

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Cite This Article

GÜNEŞ, T., DOĞAN, H., KARAMAN, B., ÖNER, A., KÖSE, M. (2022). Ocular findings in a case with Hallermann-streiff syndrome. Erciyes Tıp Dergisi, Cilt: 25 - Sayı: 4, 208–210. https://ajindex.com/articles/502858

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References (12)

  1. Soriano JM, Funk J. Spontaneous bilateral lens resorption in a case of Hallermann-Streiff syndrome. Klin Monatsbl Augenheilkd 1991; 199: 195-8. 2. da Fonseca MA, Mueller WA. Hallermann- Streiff syndrome: case report and recommendations for dental care. ASDC J Dent Child 1994; 61: 334-7
  2. Romeo MG, Betta P, Rodono A, Tina LG, Di Bella D, D'Amico P, Distefano G. A case of Hallermann-Streiff syndrome with rapidly fatal course. Pediatr Med Chir 1995; 17: 365-8
  3. 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
  4. Sato M, Terasaki H, Amano E, Okamoto Y, Miyake Y. Ultrasound biomicroscopic findings in Hallermann-streiff syndrome. Jpn J Ophthalmol 2002; 46: 451-4
  5. Nicholson AD, Menon S. Hallermann-Streiff syndrome. J Postgrad Med 1995;41: 22-3
  6. Blair NP, Brockhurst RJ, Lee W. Central serous choroidopathy in the Hallermann-Streiff Syndrome. Ann Ophthalmol 1981;13: 987-90
  7. Schanzlin DJ, Goldberg DB, Brown SI. Hallermann-Streiff syndrome associated with sclerocornea, aniridia, and a chromosomal abnormality. Am J Ophthalmol 1980; 90: 411-5
  8. Spaepen A, Schrander-Stumpel C, Fryns JP, de Die-Smulders C, Borghgraef M, Van den Berghe H. Hallermann-Streiff syndrome: clinical and psychological findings in children Nosologic overlap with oculodentodigital dysplasia? Am J Med Genet 1991; 41: 517-20
  9. Salbert BA, Stevens CA, Spence JE. Tracheomalacia in Hallermann-Streiff syndrome. Am J Med Genet 1991; 41: 521-3
  10. 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: 517-20
  11. Gerinec A, Spissakova B, Chynoransky M. The Hallermann-Streiff syndrome in 2 generations. Cesk Oftalmol 1989; 45: 326-33
  12. Imamura S, Ikeda E, Yoshida H. Hallermann- Streiff syndrome. Dermatologica 1980; 160: 354-7.