DOI: 10.1302/0301-620x.45b2.292. HEREDITARY MULTIPLE EXOSTOSIS

10.1302/0301-620x.45b2.292

Crossref journal-article

British Editorial Society of Bone & Joint Surgery

The Journal of Bone and Joint Surgery. British volume (42)

Abstract

1. Hereditary multiple exostosis has been studied in fifty-six patients and their relatives. In most cases previous records were available and the progress of the disease could be traced over many years. 2. The characteristic lesions are described and the complications encountered in the present series of cases are noted. The disease is inherited in approximately two-thirds of the cases and invariably produces detectable lesions in the heterozygote. 3. The cartilage-capped exostoses are confined to the endochondral skeleton where their incidence is closely related to the growth potential of the sites involved. 4. An attempt has been made to explain the curious distribution of the exostoses, and the likely theories of the pathogenesis of the disease are discussed.

Bibliography

Solomon, L. (1963). HEREDITARY MULTIPLE EXOSTOSIS. The Journal of Bone and Joint Surgery. British Volume, 45-B(2), 292â304.

Authors 1

L. Solomon (first)

References 0 Referenced 205

None

Dates

Type	When
Created	7 years, 6 months ago (Feb. 21, 2018, 6:25 a.m.)
Deposited	4 years ago (Aug. 16, 2021, 5:57 p.m.)
Indexed	3 weeks, 6 days ago (Aug. 5, 2025, 8:46 a.m.)
Issued	62 years, 4 months ago (May 1, 1963)
Published	62 years, 4 months ago (May 1, 1963)
Published Print	62 years, 4 months ago (May 1, 1963)

Funders 0

None

BibTeX

@article{Solomon_1963, title={HEREDITARY MULTIPLE EXOSTOSIS}, volume={45-B}, ISSN={2044-5377}, url={http://dx.doi.org/10.1302/0301-620x.45b2.292}, DOI={10.1302/0301-620x.45b2.292}, number={2}, journal={The Journal of Bone and Joint Surgery. British volume}, publisher={British Editorial Society of Bone & Joint Surgery}, author={Solomon, L.}, year={1963}, month=may, pages={292–304} }

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