- 関
- progressive diaphyseal dysplasia
WordNet
- an impairment of health or a condition of abnormal functioning
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 病気にかかった / 病的な,不健全な(morbid)
UpToDate Contents
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English Journal
- Heritable sclerosing bone disorders: presentation and new molecular mechanisms.
- de Vernejoul MC, Kornak U.SourceUniversity Paris 7, Federation of Rheumatology, Hospital Lariboisière, Paris, France. christine.devernejoul@lrb.aphp.fr
- Annals of the New York Academy of Sciences.Ann N Y Acad Sci.2010 Mar;1192:269-77. doi: 10.1111/j.1749-6632.2009.05244.x.
- Sclerosing bone disorders can be subdivided according to their clinical presentation, the primarily affected cell type, and the cellular pathways. Osteoclast-rich osteopetrosis and related disorders have been related in most cases to mutations in genes required for osteoclast function. More recently
- PMID 20392246
- Sclerosing bone disorders.
- de Vernejoul MC.SourceINSERM U606 and University Paris 7, Rheumatology Department, Hospital Lariboisière, Assistance Publique Hôpitaux de Paris, 2 rue Ambroise Paré, 75010 Paris, France. christine.devernejoul@lrb.aphp.fr
- Best practice & research. Clinical rheumatology.Best Pract Res Clin Rheumatol.2008 Mar;22(1):71-83. doi: 10.1016/j.berh.2007.12.011.
- Sclerosing bone disorders are a diagnostic challenge. However, hereditary sclerosing disorders often have characteristic radiological features that allow their diagnosis. Osteocondensation can result from decreased bone resorption; malignant recessive osteopetroses have been related to mutations in
- PMID 18328982
- [Progressive diaphyseal dysplasia: Camurati-Engelman disease].
- Nikolić D, Jovanović Z.
- Vojnosanitetski pregled. Military-medical and pharmaceutical review.Vojnosanit Pregl.1983 May-Jun;40(3):204-7.
- PMID 6636598
Related Links
- 1. J Pediatr Endocrinol Metab. 2013 Jul 12:1-7. doi: 10.1515/jpem-2013-0150. [Epub ahead of print] A family with Camurati-Engelman disease: the role of the missense p.R218C mutation in TGFbeta1 in bones and endocrine glands.
- 1. J Pediatr Endocrinol Metab. 2013 May 17:1-7. doi: 10.1515/jpem-2013-0019. [Epub ahead of print] A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands.
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- 疾患:illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 関
- ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness
- disease ≠ illness ≠ disorder