特発性足根手根骨溶解症
WordNet
- (of diseases) arising from an unknown cause; "idiopathic epilepsy"
- lysis of bone caused by disease or infection or inadequate blood supply
PrepTutorEJDIC
- 特発性疾患の(病気の原因があいまいな,また不明な場合)
UpToDate Contents
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English Journal
- Unspecific, idiopathic isolated osteolysis (Gorham-Stout syndrome) of the mandibular condylar process with its radiological, histological and clinical features: a case report and review of literature.
- Scheller K1, Herrmann-Trost P, Diesel L, Busse C, Heinzelmann C.
- Oral and maxillofacial surgery.Oral Maxillofac Surg.2014 Mar;18(1):75-9. doi: 10.1007/s10006-013-0394-5. Epub 2013 Feb 3.
- BACKGROUND: The unspecific, idiopathic isolated osteolysis is a rare condition in the various known osteopathies and better known as Gorham-Stout syndrome (Gorham's disease, GD). It belongs to the primary idiopathic osteolysis, and its aetiology is poorly understood. Many different localisations hav
- PMID 23378037
- High complication rate in revision total hip arthroplasty in juvenile idiopathic arthritis.
- Goodman SB1, Hwang K, Imrie S.
- Clinical orthopaedics and related research.Clin Orthop Relat Res.2014 Feb;472(2):637-44. doi: 10.1007/s11999-013-3326-7.
- BACKGROUND: Revision total hip arthroplasty (THA) in patients with juvenile idiopathic arthritis (JIA) is challenging as a result of the patient's young age, systemic disease, multiple affected joints, small proportions, and bone loss. The intermediate- to long-term results of these surgeries remain
- PMID 24136805
- Gruener G1, Camacho P2.
- Handbook of clinical neurology.Handb Clin Neurol.2014;119:529-40. doi: 10.1016/B978-0-7020-4086-3.00034-5.
- Paget's disease is an osteoclastic-mediated disorder of bone that results in abnormal bone resorption associated with inadequate remodeling that leads to mechanically weakened bone. Demonstrating variable geographic prevalence, it is becoming less frequent and age of onset is lengthening in areas of
- PMID 24365317
Related Links
- Idiopathic Phalangeal Osteolysis Gail Todd, FFDerm(SA), PhD, Norma Saxe, FFDerm(SA) Background:The acro-osteolyticdiseases are a heter-ogeneousgroup ofbone disorderscharacterizedbybone resorption. Acquired and genetic forms have been well
- FAMILIAL NEUROGENIC ACRO-OSTEOLYSIS I iI [II IV / Fig. 4. Pedigree tree of kindred I. 53 Fig. 5. External appearance of the feet. toe. These affections had been diagnosed as chronic suppurative osteomyelitis by
★リンクテーブル★
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- 英
- idiopathic tarsocarpal osteolysis
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- 関
- agnogenic、cryptogenic、idiopathy
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- 同
- 骨破壊