Familial tarda type osteogenesis imperfecta with dentinogenesis imperfecta Type I. Case report

Australian Dental Journal

Volumn 42, Issue 3, 1997, Pages 175-177

  Ogunsalu, Christopher ^a   Hanchard, Barrie ^b  

^a Ministry of Health   (Jamaica)

^b UNIVERSITY OF THE WEST INDIES   (Jamaica)

Author keywords

Case report; Dentinogenesis imperfecta Type I; Osteogenesis imperfecta

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CLASSIFICATION; CONGENITAL MALFORMATION; ENAMEL; FEMALE; GENETICS; HUMAN; HYPODONTIA; MOLAR TOOTH; OSTEOGENESIS IMPERFECTA; PATHOLOGY; PEDIGREE; TOOTH MALFORMATION; TOOTH PULP;

ADOLESCENT; ANODONTIA; DENTAL ENAMEL; DENTAL PULP; DENTINOGENESIS IMPERFECTA; FEMALE; HUMANS; MOLAR; OSTEOGENESIS IMPERFECTA; PEDIGREE;

EID: 0031160731     PISSN: 00450421     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1834-7819.1997.tb00117.x     Document Type: Article

References (4)

1. Clergean-Guerithault S, Jasmin JR. Dentinogenesis imperfecta Type III: Enamel and cementum defects Oral Surg Oral Med Oral Pathol 1985;59:505.
2. Lynch MA. Burket's oral medicine. Diagnosis and treatment. 8th edn Philadelphia. JB Lippincott, 1984:540.
3. Rushton M. A new form of dentinal dysplasia. Shell teeth. Oral Surg Oral Med Oral Pathol 1954;7:543-9.
4. Witkop CJ. Hereditary defects in dentin. Dent Clin North Am 1975;19:25-45.