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Article detail · 2017

Dental Findings in Marfan Syndrome: A Case Report

Journal of Istanbul University Faculty of Dentistry

YÖKSİS OpenAlex Open access · diamond TR Index Citations 7 Percentile 78.9% FWCI 1.05
Year
2017
ISSN
2149-4592
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

English (OpenAlex)

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.

Topics

  • Connective tissue disorders research
  • Cardiac Valve Diseases and Treatments
  • Aortic Disease and Treatment Approaches

Primary topic Connective tissue disorders research

Authors

  1. BÜŞRA AKKAYA
  2. EMRE KORKUT KARABÜK ÜNİVERSİTESİ
  3. NİMET ÜNLÜ SELÇUK ÜNİVERSİTESİ