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Oral findings in osteogenesis imperfecta.
Oral Surg Oral Med Oral Pathol. 1984 Feb; 57(2):161-7.OS

Abstract

The dentitions of twenty-eight patients, each of whom had either an autosomal dominant or a sporadic osteogenesis imperfecta (OI) syndrome, were evaluated. The diagnosis of dentinogenesis imperfecta (DI) could be established in all seven patients with dominantly inherited OI in three families, while all eight persons with dominant OI in three other families had normal teeth. Of the thirteen remaining patients with OI, twelve had no family history of the disorder; four had DI and eight had normal teeth. One person had a family history of OI and DI. All patients with abnormal tooth wear and spontaneous tooth fractures had DI. The DMF ratio increased with age in all patients with OI type I and was higher among the patients with OI type III and DI. Class III malocclusions were found in 66% of the patients. A statistically significant high incidence of impacted first and second molars was noted.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

6583624

Citation

Schwartz, S, and P Tsipouras. "Oral Findings in Osteogenesis Imperfecta." Oral Surgery, Oral Medicine, and Oral Pathology, vol. 57, no. 2, 1984, pp. 161-7.
Schwartz S, Tsipouras P. Oral findings in osteogenesis imperfecta. Oral Surg Oral Med Oral Pathol. 1984;57(2):161-7.
Schwartz, S., & Tsipouras, P. (1984). Oral findings in osteogenesis imperfecta. Oral Surgery, Oral Medicine, and Oral Pathology, 57(2), 161-7.
Schwartz S, Tsipouras P. Oral Findings in Osteogenesis Imperfecta. Oral Surg Oral Med Oral Pathol. 1984;57(2):161-7. PubMed PMID: 6583624.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Oral findings in osteogenesis imperfecta. AU - Schwartz,S, AU - Tsipouras,P, PY - 1984/2/1/pubmed PY - 1984/2/1/medline PY - 1984/2/1/entrez SP - 161 EP - 7 JF - Oral surgery, oral medicine, and oral pathology JO - Oral Surg Oral Med Oral Pathol VL - 57 IS - 2 N2 - The dentitions of twenty-eight patients, each of whom had either an autosomal dominant or a sporadic osteogenesis imperfecta (OI) syndrome, were evaluated. The diagnosis of dentinogenesis imperfecta (DI) could be established in all seven patients with dominantly inherited OI in three families, while all eight persons with dominant OI in three other families had normal teeth. Of the thirteen remaining patients with OI, twelve had no family history of the disorder; four had DI and eight had normal teeth. One person had a family history of OI and DI. All patients with abnormal tooth wear and spontaneous tooth fractures had DI. The DMF ratio increased with age in all patients with OI type I and was higher among the patients with OI type III and DI. Class III malocclusions were found in 66% of the patients. A statistically significant high incidence of impacted first and second molars was noted. SN - 0030-4220 UR - https://www.unboundmedicine.com/medline/citation/6583624/Oral_findings_in_osteogenesis_imperfecta_ L2 - http://www.diseaseinfosearch.org/result/5451 DB - PRIME DP - Unbound Medicine ER -