مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

DENTAL MANAGEMENT OF A CHILD WITH DENTINOGENESIS IMPERFECTA: A CASE REPORT

Pages

  133-138

Abstract

DENTINogenesis imperfecta (DI) is a hereditary DENTIN defect caused by an autosomal dominant mutation in DENTIN sialophosphoprotein gene. Defective DENTIN development results in discolored teeth that are prone to wear and fracture. Early diagnosis and proper treatment are necessary to achieve better functional and esthetic results and minimize nutritional deficiencies and psychosocial distress. In order to prevent excessive loss of TOOTH structure, placement of stainless steel crowns (SSCs) on DECIDUOUS and young permanent posterior teeth is recommended as soon as such teeth erupt. This clinical report presents the clinical manifestations and management of a 3.5-year-old child diagnosed with DI type II.

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  • References

    Cite

    APA: Copy

    AKHLAGHI, NAJMEH, ESHGHI, ALI REZA, & MOHAMMADPOUR, MEHRNAZ. (2016). DENTAL MANAGEMENT OF A CHILD WITH DENTINOGENESIS IMPERFECTA: A CASE REPORT. FRONTIERS IN DENTISTRY (JOURNAL OF DENTISTRY OF TEHRAN UNIVERSITY OF MEDICAL SCIENCES), 13(2), 133-138. SID. https://sid.ir/paper/298045/en

    Vancouver: Copy

    AKHLAGHI NAJMEH, ESHGHI ALI REZA, MOHAMMADPOUR MEHRNAZ. DENTAL MANAGEMENT OF A CHILD WITH DENTINOGENESIS IMPERFECTA: A CASE REPORT. FRONTIERS IN DENTISTRY (JOURNAL OF DENTISTRY OF TEHRAN UNIVERSITY OF MEDICAL SCIENCES)[Internet]. 2016;13(2):133-138. Available from: https://sid.ir/paper/298045/en

    IEEE: Copy

    NAJMEH AKHLAGHI, ALI REZA ESHGHI, and MEHRNAZ MOHAMMADPOUR, “DENTAL MANAGEMENT OF A CHILD WITH DENTINOGENESIS IMPERFECTA: A CASE REPORT,” FRONTIERS IN DENTISTRY (JOURNAL OF DENTISTRY OF TEHRAN UNIVERSITY OF MEDICAL SCIENCES), vol. 13, no. 2, pp. 133–138, 2016, [Online]. Available: https://sid.ir/paper/298045/en

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