Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1991 Apr;28(4):262–266. doi: 10.1136/jmg.28.4.262

Hereditary multiple exostoses.

R C Hennekam 1
PMCID: PMC1016830  PMID: 1856833

Full text

PDF
262

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Beighton P., Christy G., Learmonth I. D. Namaqualand hip dysplasia: an autosomal dominant entity. Am J Med Genet. 1984 Sep;19(1):161–169. doi: 10.1002/ajmg.1320190116. [DOI] [PubMed] [Google Scholar]
  2. Buur T., Mørch M. M. Hereditary multiple exostoses with spinal cord compression. J Neurol Neurosurg Psychiatry. 1983 Jan;46(1):96–98. doi: 10.1136/jnnp.46.1.96-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bühler E. M., Malik N. J. The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities? Am J Med Genet. 1984 Sep;19(1):113–119. doi: 10.1002/ajmg.1320190111. [DOI] [PubMed] [Google Scholar]
  4. Callan J. E., Wood V. E., Linda L. Spontaneous resolution of an osteochondroma. J Bone Joint Surg Am. 1975 Jul;57(5):723–723. [PubMed] [Google Scholar]
  5. Canella P., Gardini F., Boriani S. Exostosis: development, evolution and relationship to malignant degeneration. Ital J Orthop Traumatol. 1981 Dec;7(3):293–298. [PubMed] [Google Scholar]
  6. Chiurco A. A. Multiple exostoses of bone with fatal spinal cord compression; report of a case and brief review of the literature. Neurology. 1970 Mar;20(3):275–278. doi: 10.1212/wnl.20.3.275. [DOI] [PubMed] [Google Scholar]
  7. Copeland R. L., Meehan P. L., Morrissy R. T. Spontaneous regression of osteochondromas. Two case reports. J Bone Joint Surg Am. 1985 Jul;67(6):971–973. [PubMed] [Google Scholar]
  8. Fuchs G. A. Multiple kartilaginäre Exostosen bei Kolon- und Magen-Polypose. Mitteilungen einer neuen, vom Gardner-Syndrom abweichenden erblichen Kombinationserkrankung. Dtsch Med Wochenschr. 1975 Nov 7;100(45):2316–2319. doi: 10.1055/s-0028-1106541. [DOI] [PubMed] [Google Scholar]
  9. Gardner E. J., Shupe J. L., Leone N. C., Olson A. E. Hereditary multiple exostosis. A comparative genetic evaluation in man and horses. J Hered. 1975 Nov-Dec;66(6):318–326. doi: 10.1093/oxfordjournals.jhered.a108640. [DOI] [PubMed] [Google Scholar]
  10. Goodman R. M., Lewithal I., Solomon A., Klein D. Upper limb involvement in the Klein-Waardenburg syndrome. Am J Med Genet. 1982 Apr;11(4):425–433. doi: 10.1002/ajmg.1320110407. [DOI] [PubMed] [Google Scholar]
  11. Gorlin R. J., Winter R. B. Frontometaphyseal dysplasia--evidence for X-linked inheritance. Am J Med Genet. 1980;5(1):81–84. doi: 10.1002/ajmg.1320050111. [DOI] [PubMed] [Google Scholar]
  12. HAMRE C. J., YEAGER V. L. Influence of denervated muscles on exostoses of rats fed a sweet-pea diet. AMA Arch Pathol. 1958 Feb;65(2):215–227. [PubMed] [Google Scholar]
  13. Hall J. G. Genomic imprinting: review and relevance to human diseases. Am J Hum Genet. 1990 May;46(5):857–873. [PMC free article] [PubMed] [Google Scholar]
  14. Hall J. G., Wilson R. D., Kalousek D., Beauchamp R. Familial multiple exostoses--no chromosome 8 deletion observed. Am J Med Genet. 1985 Nov;22(3):639–640. doi: 10.1002/ajmg.1320220328. [DOI] [PubMed] [Google Scholar]
  15. Hamers A., Jongbloet P., Peeters G., Fryns J. P., Geraedts J. Severe mental retardation in a patient with tricho-rhino-phalangeal syndrome type I and 8q deletion. Eur J Pediatr. 1990 Jun;149(9):618–620. doi: 10.1007/BF02034746. [DOI] [PubMed] [Google Scholar]
  16. Hershey S. L., Lansden F. T. Osteochondromas as a cause of false popliteal aneurysms. Review of the literature and report of two cases. J Bone Joint Surg Am. 1972 Dec;54(8):1765–1768. [PubMed] [Google Scholar]
  17. Keith A. Studies on the Anatomical Changes which accompany certain Growth-disorders of the Human Body: I. The Nature of the Structural Alterations in the Disorder known as Multiple Exostoses. J Anat. 1920 Jan;54(Pt 2-3):101–115. [PMC free article] [PubMed] [Google Scholar]
  18. Kennedy L. A. Metachondromatosis. Radiology. 1983 Jul;148(1):117–118. doi: 10.1148/radiology.148.1.6602353. [DOI] [PubMed] [Google Scholar]
  19. Kettelkamp D. B., Campbell C. J., Bonfiglio M. Dysplasia epiphysealis hemimelica. A report of fifteen cases and a review of the literature. J Bone Joint Surg Am. 1966 Jun;48(4):746–766. [PubMed] [Google Scholar]
  20. Kozlowski K. S., Celermajer J. M., Tink A. R. Humero-spinal dysostosis with congenital heart disease. Am J Dis Child. 1974 Mar;127(3):407–410. doi: 10.1001/archpedi.1974.02110220105015. [DOI] [PubMed] [Google Scholar]
  21. Langer L. O., Jr, Krassikoff N., Laxova R., Scheer-Williams M., Lutter L. D., Gorlin R. J., Jennings C. G., Day D. W. The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature. Am J Med Genet. 1984 Sep;19(1):81–112. doi: 10.1002/ajmg.1320190110. [DOI] [PubMed] [Google Scholar]
  22. Leone N. C., Shupe J. L., Gardner E. J., Millar E. A., Olson A. E., Phillips E. C. Hereditary multiple exostosis. A comparative human-equine-epidemiologic study. J Hered. 1987 May-Jun;78(3):171–177. doi: 10.1093/oxfordjournals.jhered.a110351. [DOI] [PubMed] [Google Scholar]
  23. Li J. K., Moloney B. K., Shupe J. L., Gardner E. J., Leone N. C., Elsner Y. DNA polymorphism analysis of hereditary multiple exostoses in horses. Am J Vet Res. 1989 Jun;50(6):978–983. [PubMed] [Google Scholar]
  24. Li J. K., Moloney B. K., Shupe J. L., Gardner E. J., Leone N. C., Elsner Y. DNA polymorphism analysis of hereditary multiple exostoses in horses. Am J Vet Res. 1989 Jun;50(6):978–983. [PubMed] [Google Scholar]
  25. Loomer R. L. Shoulder girdle dysplasia associated with nail patella syndrome. A case report and literature review. Clin Orthop Relat Res. 1989 Jan;(238):112–116. [PubMed] [Google Scholar]
  26. Lüdecke H. J., Burdiek R., Senger G., Claussen U., Passarge E., Horsthemke B. Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome. Hum Genet. 1989 Jul;82(4):327–329. doi: 10.1007/BF00273991. [DOI] [PubMed] [Google Scholar]
  27. Mollica F., Li Volti S., Guarneri B. New syndrome: exostoses, anetodermia, brachydactyly. Am J Med Genet. 1984 Dec;19(4):665–667. doi: 10.1002/ajmg.1320190406. [DOI] [PubMed] [Google Scholar]
  28. Ochsner P. E. Zum Problem der neoplastischen Entartung bei multiplen kartilaginären Exostosen. Z Orthop Ihre Grenzgeb. 1978;116(3):369–378. [PubMed] [Google Scholar]
  29. Pascual-Castroviejo I., Santolaya J. M., Martin V. L., Rodriguez-Costa T., Tendero A., Mulas F. Cerebro-facio-thoracic dysplasia: report of three cases. Dev Med Child Neurol. 1975 Jun;17(3):343–351. doi: 10.1111/j.1469-8749.1975.tb04673.x. [DOI] [PubMed] [Google Scholar]
  30. Peterson H. A. Multiple hereditary osteochondromata. Clin Orthop Relat Res. 1989 Feb;(239):222–230. [PubMed] [Google Scholar]
  31. Proschek R., Labelle H., Bard C., Marton D. Osteomesopyknosis. Case report. J Bone Joint Surg Am. 1985 Apr;67(4):652–653. [PubMed] [Google Scholar]
  32. Reimão R., Diament A. Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis. Arq Neuropsiquiatr. 1989 Mar;47(1):76–79. doi: 10.1590/s0004-282x1989000100010. [DOI] [PubMed] [Google Scholar]
  33. SOLOMON L. HEREDITARY MULTIPLE EXOSTOSIS. Am J Hum Genet. 1964 Sep;16:351–363. [PMC free article] [PubMed] [Google Scholar]
  34. Schweitzer G., Jones B., Timme A. Upington disease: a familial dyschondroplasia. S Afr Med J. 1971 Sep 18;45(36):994–1000. [PubMed] [Google Scholar]
  35. Shapiro F., Simon S., Glimcher M. J. Hereditary multiple exostoses. Anthropometric, roentgenographic, and clinical aspects. J Bone Joint Surg Am. 1979 Sep;61(6A):815–824. [PubMed] [Google Scholar]
  36. Shupe J. L., Leone N. C., Olson A. E., Gardner E. J. Hereditary multiple exostoses: clinicopathologic features of a comparative study in horses and man. Am J Vet Res. 1979 Jun;40(6):751–757. [PubMed] [Google Scholar]
  37. Stoll C. G., Collin D., Dreyfus J. Osteomesopyknosis: an autosomal dominant osteosclerosis. Am J Med Genet. 1981;8(3):349–353. doi: 10.1002/ajmg.1320080314. [DOI] [PubMed] [Google Scholar]
  38. Voutsinas S., Wynne-Davies R. The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. J Med Genet. 1983 Oct;20(5):345–349. doi: 10.1136/jmg.20.5.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Wood V. E., Sauser D., Mudge D. The treatment of hereditary multiple exostosis of the upper extremity. J Hand Surg Am. 1985 Jul;10(4):505–513. doi: 10.1016/s0363-5023(85)80074-5. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES