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. 1990 Nov;27(11):701–706. doi: 10.1136/jmg.27.11.701

Craniodiaphyseal dysplasia.

L A Brueton 1, R M Winter 1
PMCID: PMC1017262  PMID: 2277386

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Selected References

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

  1. Bonucci E., Menichini G., Scarfó G. B., Tomaccini D. Histologic, microradiographic and electron microscopic investigations of bone tissue in a case of craniodiaphyseal dysplasia. Virchows Arch A Pathol Anat Histol. 1977 Mar 11;373(2):167–175. doi: 10.1007/BF00432161. [DOI] [PubMed] [Google Scholar]
  2. Itagaki Y., Sakamoto M., Nishitani H. [A case of craniodiaphyseal dysplasia]. No To Hattatsu. 1989 Jan;21(1):69–73. [PubMed] [Google Scholar]
  3. Macpherson R. I. Craniodiaphyseal dysplasia, a disease or group of diseases? J Can Assoc Radiol. 1974 Mar;25(1):22–33. [PubMed] [Google Scholar]
  4. McKeating J. B., Kershaw C. R. Craniodiaphyseal dysplasia. Partial suppression of osteoblastic activity in the severe progressive form with calcitonin therapy. J R Nav Med Serv. 1987 Summer;73(2):81–93. [PubMed] [Google Scholar]
  5. Menichini G., Salvatori Q., Picotti E., Nieri G. La malattia di Camurati-Engelmann (contributo clinico e radiologico. Minerva Pediatr. 1972 May 12;24(17):697–701. [PubMed] [Google Scholar]
  6. Menichini G., Scarfò G. B., Cantore G. P., Marchetti P. G., Tomaccini D. Singolare caso di malattia iperostosica del tipo "displasia cranio-diafisaria". Minerva Pediatr. 1977 Jul 14;29(23):1485–1497. [PubMed] [Google Scholar]
  7. STRANSKY E., MABILANGAN L., LARA R. T. On Paget's disease with leontiasis ossea and hypothyreosis, starting in early childhood. Ann Paediatr. 1962;199:393–408. [PubMed] [Google Scholar]
  8. Scarfò G. B., Tomaccini D., Capaccioli L., Gambacorta D. Idrocefalo associato a displasia cranio-diafisaria. Radiol Med. 1979 Apr;65(4):249–252. [PubMed] [Google Scholar]
  9. Schaefer B., Stein S., Oshman D., Rennert O., Thurnau G., Wall J., Bodensteiner J., Brown O. Dominantly inherited craniodiaphyseal dysplasia: a new craniotubular dysplasia. Clin Genet. 1986 Nov;30(5):381–391. doi: 10.1111/j.1399-0004.1986.tb01895.x. [DOI] [PubMed] [Google Scholar]
  10. Sparkes R. S., Graham C. B. Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature. J Med Genet. 1972 Mar;9(1):73–85. doi: 10.1136/jmg.9.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. VAN BUCHEM F. S., HADDERS H. N., HANSEN J. F., WOLDRING M. G. Hyperostosis corticalis generalisata. Report of seven cases. Am J Med. 1962 Sep;33:387–397. doi: 10.1016/0002-9343(62)90235-8. [DOI] [PubMed] [Google Scholar]

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