KaydedilenlerDerginizi ekleyin

Dergiler / European Oral Research / 2017 / Cilt: 51 - Sayı: 2

DENTAL FINDINGS IN MARFAN SYNDROME: A CASE REPORT

Büşra BOSTANCI
Nimet ÜNLÜ
Emre KORKUT
Sayfa
61–67
Yayın Tarihi
2017-04-02
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The patient was advised to visit regularly for follow up and she was referred for orthodontic evaluation.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Marfan syndrome is an autosomal dominant disorder of connective tissue primarily characterized with anomalies affecting the musculoskeletal system, the cardiovascular system and the eyes.
📊
Temel Bulgular & Veri:A 7-year-old female was referred to our clinic, with a chief complaint of dental crowding in the anterior region of mandible.
💡
Sonuç & Katkı:The patient was advised to visit regularly for follow up and she was referred for orthodontic evaluation.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Marfan syndrome · dental management · antibiotic prophylaxis

Abstract

Marfan syndrome is an autosomal dominant disorder of connective tissue primarily characterized with anomalies affecting the musculoskeletal system, the cardiovascular system and the eyes. It has been suggested that early diagnosis of the syndrome is important, because of the risk of infective endocarditis. A 7-year-old female was referred to our clinic, with a chief complaint of dental crowding in the anterior region of mandible. It was observed that the patient needed multiple treatments based on detailed clinical and radiographic examinations. The treatment was carried out with antibiotic prophylaxis an hour prior to her appointment considering her profound caries. The patient was advised to visit regularly for follow up and she was referred for orthodontic evaluation.

🔖

Bu Makaleye Atıf Yap

BOSTANCI, B., ÜNLÜ, N., KORKUT, E. (2017). DENTAL FINDINGS IN MARFAN SYNDROME: A CASE REPORT. European Oral Research, Cilt: 51 - Sayı: 2, 61–67. https://ajindex.com/articles/243018

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (14)

  1. McKusick VA. Heritable disorders of connective tissue. III. The Marfan syndrome. J Chronic Dis 1955;2(6):609-644.
  2. Shirley ED, Sponseller PD. Marfan syndrome. J Am Acad Orthop Surg 2009;17(9):572-581.
  3. Dietz HC, Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A, Nanthakumar EJ, Curristin SM, et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 1991;352(6333):337-339.
  4. Hirst AE, Jr., Gore I. Marfan's syndrome: A review. Prog Cardiovasc Dis 1973;16(2):187-198.
  5. Rybczynski M, Bernhardt AM, Rehder U, Fuisting B, Meiss L, Voss U, Habermann C, Detter C, Robinson PN, Arslan-Kirchner M, Schmidtke J, Mir TS, Berger J, Meinertz T, von Kodolitsch Y. The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome. Am J Med Genet A 2008;146A(24):3157-3166. Dean JC. Management of Marfan syndrome. Heart 2002;88(1):97-103.
  6. Maslen CL, Corson GM, Maddox BK, Glanville RW, Sakai LY. Partial sequence of a candidate gene for the Marfan syndrome. Nature 1991;352(6333):334-337.
  7. Biros E, Walker PJ, Nataatmadja M, West M, Golledge J. Downregulation of transforming growth factor, beta receptor 2 and notch signaling pathway in human abdominal aortic aneurysm. Atherosclerosis 2012;221(2):383-386.
  8. Grimes SJ, Acheson LS, Matthews AL, Wiesner GL. Clinical consult: Marfan syndrome. Prim Care 2004;31(3):739-742.
  9. Loeys BL, Dietz HC, Braverman AC, Callewaert BL, De Backer J, Devereux RB, Hilhorst-Hofstee Y, Jondeau G, Faivre L, Milewicz DM, Pyeritz RE, Sponseller PD, Wordsworth P, De Paepe AM. The revised ghent nosology for the marfan syndrome. J Med Genet 2010;47(7):476-485.
  10. De Coster PJ, Martens LC, De Paepe A. Oral manifestations of patients with Marfan syndrome: A case-control study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002;93(5):564-572.
  11. Utreja A, Evans CA. Marfan syndrome-an orthodontic perspective. Angle Orthod 2009;79(2):394-400.
  12. Westling L, Mohlin B, Bresin A. Craniofacial manifestations in the marfan syndrome: Palatal dimensions and a comparative cephalometric analysis. J Craniofac Genet Dev Biol 1998;18(4):211-218.
  13. S. Judith, F. Rebecca, T. Gale, “Marfan Syndrome,” Gale Encyclopedia of Children's Health: Infancy through Adolescence, 2006. Available from: http://www.encyclopedia.com/topic/Marfan_Syndrome.aspx.
  14. Jaiswal S, Magar BS, Poudel M, Joshi LN, Neopane A, Karki DB. Marfan's syndrome with aortic valve endocarditis. Kathmandu Univ Med J (KUMJ) 2004;2(3):23