Exostosis cartilaginea multiplex két esete egy családban.

Translated title of the contribution: Two familial cases of hereditary multiple exostoses

P. Géher, K. Csauth, N. P. Kaposi

Research output: Contribution to journalArticle

Abstract

Hereditary multiple exostoses is an autosomal dominant disorder. Three different chromosomal loci have been implicated in this genetically heterogeneous disease. The authors describe a family in which 3 generations were affected, there were data about the disease of an already died grandmother, the father and his daughter were investigated by conventional X-ray and the disease was proved. The disease caused only minor complaints. The exostosis of the father's pelvis showed increased isotope uptake during bone scintigraphic examination, the same region exhibited malignant degeneration on MR examination. Regular check-up of the patients is necessary because of the possibility to a malignant transformation in 1-27% of the cases.

Original languageHungarian
Pages (from-to)289-293
Number of pages5
JournalOrvosi Hetilap
Volume141
Issue number6
Publication statusPublished - Feb 6 2000

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Multiple Hereditary Exostoses
Fathers
Exostoses
Pelvis
Nuclear Family
Isotopes
X-Rays
Bone and Bones

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Géher, P., Csauth, K., & Kaposi, N. P. (2000). Exostosis cartilaginea multiplex két esete egy családban. Orvosi Hetilap, 141(6), 289-293.

Exostosis cartilaginea multiplex két esete egy családban. / Géher, P.; Csauth, K.; Kaposi, N. P.

In: Orvosi Hetilap, Vol. 141, No. 6, 06.02.2000, p. 289-293.

Research output: Contribution to journalArticle

Géher, P, Csauth, K & Kaposi, NP 2000, 'Exostosis cartilaginea multiplex két esete egy családban.', Orvosi Hetilap, vol. 141, no. 6, pp. 289-293.
Géher, P. ; Csauth, K. ; Kaposi, N. P. / Exostosis cartilaginea multiplex két esete egy családban. In: Orvosi Hetilap. 2000 ; Vol. 141, No. 6. pp. 289-293.
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