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Osteogenesis imperfecta with unusual skeletal lesions: report of three families.
Am J Med Genet. 1985 Jun; 21(2):257-69.AJ

Abstract

Thirteen individuals with osteogenesis imperfecta (OI) from three families were evaluated. All examined persons with OI had multilocular radiolucent, radiopaque, or radiolucent-radiopaque lesions of the maxilla and mandible. In most patients, the lesions involved the tooth bearing areas, but in two, the rami also were involved. Teeth were normal. Radiologic findings in the extragnathic skeleton included marked coarseness of trabeculae and diffuse osteopenia. It is proposed that these patients represent yet another dominantly inherited OI syndrome.

Authors

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Pub Type(s)

Case Reports
Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

4014312

Citation

Levin, L S., et al. "Osteogenesis Imperfecta With Unusual Skeletal Lesions: Report of Three Families." American Journal of Medical Genetics, vol. 21, no. 2, 1985, pp. 257-69.
Levin LS, Wright JM, Byrd DL, et al. Osteogenesis imperfecta with unusual skeletal lesions: report of three families. Am J Med Genet. 1985;21(2):257-69.
Levin, L. S., Wright, J. M., Byrd, D. L., Greenway, G., Dorst, J. P., Irani, R. N., Pyeritz, R. E., Young, R. J., & Laspia, C. L. (1985). Osteogenesis imperfecta with unusual skeletal lesions: report of three families. American Journal of Medical Genetics, 21(2), 257-69.
Levin LS, et al. Osteogenesis Imperfecta With Unusual Skeletal Lesions: Report of Three Families. Am J Med Genet. 1985;21(2):257-69. PubMed PMID: 4014312.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Osteogenesis imperfecta with unusual skeletal lesions: report of three families. AU - Levin,L S, AU - Wright,J M, AU - Byrd,D L, AU - Greenway,G, AU - Dorst,J P, AU - Irani,R N, AU - Pyeritz,R E, AU - Young,R J, AU - Laspia,C L, PY - 1985/6/1/pubmed PY - 1985/6/1/medline PY - 1985/6/1/entrez SP - 257 EP - 69 JF - American journal of medical genetics JO - Am J Med Genet VL - 21 IS - 2 N2 - Thirteen individuals with osteogenesis imperfecta (OI) from three families were evaluated. All examined persons with OI had multilocular radiolucent, radiopaque, or radiolucent-radiopaque lesions of the maxilla and mandible. In most patients, the lesions involved the tooth bearing areas, but in two, the rami also were involved. Teeth were normal. Radiologic findings in the extragnathic skeleton included marked coarseness of trabeculae and diffuse osteopenia. It is proposed that these patients represent yet another dominantly inherited OI syndrome. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/4014312/Osteogenesis_imperfecta_with_unusual_skeletal_lesions:_report_of_three_families_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1985&volume=21&issue=2&spage=257 DB - PRIME DP - Unbound Medicine ER -