Idiopathic osteonecrosis in an adult with familial protein S deficiency and hyperhomocysteinemia

K. Elishkewich, D. Kaspi, I. Shapira, D. Meites, Shlomo Berliner*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

We describe a 36-year-old man with familial protein S deficiency and homozygosity to the methylene tetrahydrofolate reductase (MTHFR) thermolabile variant who had a stroke followed by an episode of idiopathic osteonecrosis that was successfully managed by surgical core decompression. The patient's symptomatic thrombophilia, as well as that of several of his first-degree relatives who also had thrombotic events, raises the possibility that the thrombophilia was a contributing factor to the development of his osteonecrosis.

Original languageEnglish
Pages (from-to)547-550
Number of pages4
JournalBlood Coagulation and Fibrinolysis
Volume12
Issue number7
DOIs
StatePublished - 2001
Externally publishedYes

Keywords

  • Hyperhomocysteinemia
  • Osteonecrosis
  • Protein S deficiency

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