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Pediatric dental management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta.
Spec Care Dentist. 2007 Nov-Dec; 27(6):240-5.SC

Abstract

Osteogenesis imperfecta (OI) is a genetic disorder that affects all connective tissue. Clinical manifestations of OI include bone fragility, hyperlaxity of joints, hearing loss, abnormalities of stature and facial structure, blue sclerae, and dentinogenesis imperfecta (DI). OI is classified into four groups according to the severity and physical characteristics of the disease, although not all characteristics may be present in one individual. Currently, 20,000 to 50,000 individuals in the U.S. have been diagnosed with this disease. The aim of this article is to discuss medical and dental complications associated with OI and DI. A case presentation describes the clinical care of a patient from birth to age 12.

Authors+Show Affiliations

Baylor College of Dentistry, Dallas, Texas, USA. kmuhney@bcd.tamhsc.eduNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

18683807

Citation

Muhney, Kelly, and Patricia Regener Campbell. "Pediatric Dental Management of a Patient With Osteogenesis Imperfecta and Dentinogenesis Imperfecta." Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry, vol. 27, no. 6, 2007, pp. 240-5.
Muhney K, Campbell PR. Pediatric dental management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta. Spec Care Dentist. 2007;27(6):240-5.
Muhney, K., & Campbell, P. R. (2007). Pediatric dental management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta. Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry, 27(6), 240-5.
Muhney K, Campbell PR. Pediatric Dental Management of a Patient With Osteogenesis Imperfecta and Dentinogenesis Imperfecta. Spec Care Dentist. 2007 Nov-Dec;27(6):240-5. PubMed PMID: 18683807.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pediatric dental management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta. AU - Muhney,Kelly, AU - Campbell,Patricia Regener, PY - 2008/8/8/pubmed PY - 2008/8/19/medline PY - 2008/8/8/entrez SP - 240 EP - 5 JF - Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry JO - Spec Care Dentist VL - 27 IS - 6 N2 - Osteogenesis imperfecta (OI) is a genetic disorder that affects all connective tissue. Clinical manifestations of OI include bone fragility, hyperlaxity of joints, hearing loss, abnormalities of stature and facial structure, blue sclerae, and dentinogenesis imperfecta (DI). OI is classified into four groups according to the severity and physical characteristics of the disease, although not all characteristics may be present in one individual. Currently, 20,000 to 50,000 individuals in the U.S. have been diagnosed with this disease. The aim of this article is to discuss medical and dental complications associated with OI and DI. A case presentation describes the clinical care of a patient from birth to age 12. SN - 0275-1879 UR - https://www.unboundmedicine.com/medline/citation/18683807/Pediatric_dental_management_of_a_patient_with_osteogenesis_imperfecta_and_dentinogenesis_imperfecta_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0275-1879&date=2007&volume=27&issue=6&spage=240 DB - PRIME DP - Unbound Medicine ER -