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Osteomesopyknosis. Report of two new cases.

Abstract
Two inherited cases of osteomesopyknosis are reported. This is an autosomal dominant osteosclerosis described by Maroteaux in 1980; its radiological abnormalities consist of increased density of the vertebral plates, pelvis, and sometimes of the upper part of the femur. Osteomesopyknosis, usually discovered incidentally on radiographic examination, is a mild form of familial osteosclerosis and must be distinguished from osteopetrosis which carries a worse prognosis.
AuthorsB Delcambre, R M Flipo, J L Leroux, B Duquesnoy
JournalSkeletal radiology (Skeletal Radiol) Vol. 18 Issue 1 Pg. 21-4 ( 1989) ISSN: 0364-2348 [Print] Germany
PMID2711206 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Diagnosis, Differential
  • Female
  • Genes, Dominant
  • Humans
  • Male
  • Osteopetrosis (diagnostic imaging)
  • Osteosclerosis (diagnostic imaging, genetics)
  • Radiography

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