骨形成異常、骨異栄養症
WordNet
- defective bone development; usually attributable to renal disease or to disturbances in calcium and phosphorus metabolism
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/08/23 10:12:11」(JST)
[Wiki en表示]
Osteodystrophy |
Classification and external resources |
Specialty |
medical genetics |
ICD-10 |
Q78.9 |
ICD-9-CM |
756.50 |
DiseasesDB |
31985 |
Osteodystrophy is a general term for a dystrophic growth of the bone. It is defective bone development that is usually attributable to renal disease or to disturbances in calcium and phosphorus metabolism.
One form is renal osteodystrophy.
See also
- List of radiographic findings associated with cutaneous conditions
Osteochondrodysplasia (Q77–Q78, 756.4–756.5)
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Osteodysplasia//
osteodystrophy |
Diaphysis |
- Camurati–Engelmann disease
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Metaphysis |
- Metaphyseal dysplasia
- Jansen's metaphyseal chondrodysplasia
- Schmid metaphyseal chondrodysplasia
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Epiphysis |
- Spondyloepiphyseal dysplasia congenita
- Multiple epiphyseal dysplasia
- Otospondylomegaepiphyseal dysplasia
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Osteosclerosis |
- Raine syndrome
- Osteopoikilosis
- Osteopetrosis
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Other/ungrouped |
- FLNB
- Opsismodysplasia
- Polyostotic fibrous dysplasia
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Chondrodysplasia/
chondrodystrophy
(including dwarfism) |
Osteochondroma |
- osteochondromatosis
- Hereditary multiple exostoses
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Chondroma/enchondroma |
- enchondromatosis
- Ollier disease
- Maffucci syndrome
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Growth factor receptor |
FGFR2: |
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FGFR3: |
- Achondroplasia
- Thanatophoric dysplasia
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COL2A1 collagen disease |
- Achondrogenesis
- Hypochondrogenesis
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SLC26A2 sulfation defect |
- Achondrogenesis
- Autosomal recessive multiple epiphyseal dysplasia
- Atelosteogenesis, type II
- Diastrophic dysplasia
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Chondrodysplasia punctata |
- Rhizomelic chondrodysplasia punctata
- Conradi–Hünermann syndrome
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Other dwarfism |
- Fibrochondrogenesis
- Short rib – polydactyly syndrome
- Majewski's polydactyly syndrome
- Léri–Weill dyschondrosteosis
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Index of bones and cartilage
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Description |
- Anatomy
- bones
- skull
- face
- neurocranium
- compound structures
- foramina
- upper extremity
- torso
- pelvis
- lower extremity
- Physiology
- Development
- Cells
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Disease |
- Congenital
- Neoplasms and cancer
- Trauma
- Other
- Symptoms and signs
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Treatment |
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UpToDate Contents
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English Journal
- Serum levels of innate immunity cytokines are elevated in dogs with metaphyseal osteopathy (hypertrophic osteodytrophy) during active disease and remission.
- Safra N1, Hitchens PL2, Maverakis E3, Mitra A3, Korff C4, Johnson E4, Kol A4, Bannasch MJ4, Pedersen NC4, Bannasch DL4.
- Veterinary immunology and immunopathology.Vet Immunol Immunopathol.2016 Oct 15;179:32-5. doi: 10.1016/j.vetimm.2016.08.003. Epub 2016 Aug 3.
- Metaphyseal osteopathy (MO) (hypertrophic osteodystrophy) is a developmental disorder of unexplained etiology affecting dogs during rapid growth. Affected dogs experience relapsing episodes of lytic/sclerotic metaphyseal lesions and systemic inflammation. MO is rare in the general dog population; ho
- PMID 27590423
- Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletion.
- de Lange IM1, Verrijn Stuart AA2, van der Luijt RB1, Ploos van Amstel HK1, van Haelst MM1.
- American journal of medical genetics. Part A.Am J Med Genet A.2016 Sep;170(9):2431-5. doi: 10.1002/ajmg.a.37818. Epub 2016 Jun 23.
- Pseudohypoparathyroidism (PHP) is a genetic disorder with resistance to parathyroid hormone (PTH) as most important feature. Main subtypes of the disease are pseudohypoparathyroidism 1b (PHP1b) and pseudohypoparathyroidism 1a (PHP1a). PHP1b is characterized by PTH resistance of the renal cortex due
- PMID 27338644
- [Bone turnover and mineralization in patients with kidney failure].
- James J1.
- Clinical calcium.Clin Calcium.2016 Sep;26(9):1261-7. doi: CliCa160912611267.
- Bone remodeling is a device to accomplish "the buffering of the extracellular fluid mineral", which is one of the two major physiological functions of bone. Bone turnover is a term to express the frequency of bone remodeling, and its last step is calcification. When remodeling is induced, at first a
- PMID 27561340
Japanese Journal
- No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity
- Izzi Benedetta,Zegher Francis de,Francois Inge [他],DEL FAVERO Jurgen,GOOSSENS Dirk,WITTEVRONGEL Christine,THYS Chantal,VAN GEET Chris,FRESON Kathleen
- Journal of human genetics 57(4), 277-279, 2012-04-01
- NAID 10030662897
- Reproducibility and agreement of micro-CT and histomorphometry in human trabecular bone with different metabolic status
- TAMMINEN Inari S.,ISAKSSON Hanna,AULA Antti S.,HONKANEN Eero,JURVELIN Jukka S.,KROGER Heikki
- Journal of bone and mineral metabolism 29(4), 442-448, 2011-07-30
- NAID 10029298980
- Comparative study of quantitative ultrasonography and dual-energy X-ray absorptiometry for evaluating renal osteodystrophy in children with chronic kidney disease
- CHRISTOFORIDIS Athanasios,PRINTZA Nikoleta,GKOGKA Chrysa,SIOMOU Ekaterini,CHALLA Anna,KAZANTZIDOU Eirini,KOLLIOS Konstantinos,PAPACHRISTOU Fotis
- Journal of bone and mineral metabolism 29(3), 321-327, 2011-05-30
- NAID 10029024791
Related Pictures
★リンクテーブル★
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- 英
- osteodystrophy
- ラ
- osteodystrophia
- 同
- 骨ジストロフィー、骨形成異常症
- 関
- 骨形成異常
[★]
- 英
- osteodystrophy
- 関
- 骨異栄養症
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腎性骨ジストロフィー 腎性骨異栄養症 renal osteodystrophy。腎性骨症
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オルブライト遺伝性骨異栄養症