骨粗鬆症・偽性神経膠腫症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- abnormal loss of bony tissue resulting in fragile porous bones attributable to a lack of calcium; most common in postmenopausal women
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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English Journal
- Fractures on bisphosphonates in osteoporosis pseudoglioma syndrome (OPPG): pQCT shows poor bone density and structure.
- Streeten EA1, Ramirez S2, Eliades M2, Jaimungal S2, Chandrasekaran S2, Kathleen R2, Holmes Morton D3, Puffenberger EG3, Herskovitz R4, Leonard MB4.
- Bone.Bone.2015 Aug;77:17-23. doi: 10.1016/j.bone.2015.04.007. Epub 2015 Apr 16.
- Osteoporosis pseudoglioma syndrome (OPPG) is a rare autosomal recessive disorder of childhood osteoporosis and blindness due to inactivating mutations in LDL receptor-like protein 5 (LRP5). We and others have reported improvement in areal bone mineral density (aBMD) by DXA in OPPG on short term bisp
- PMID 25892485
- LRP receptor family member associated bone disease.
- Lara-Castillo N1, Johnson ML.
- Reviews in endocrine & metabolic disorders.Rev Endocr Metab Disord.2015 Jun;16(2):141-8. doi: 10.1007/s11154-015-9315-2.
- A dozen years ago the identification of causal mutations in the low-density lipoprotein receptor-related protein 5 (LRP5) gene involved in two rare bone disorders propelled research in the bone field in totally new directions. Since then, there have been an explosion in the number of reports that hi
- PMID 26048454
- Atypical femoral fracture in osteoporosis pseudoglioma syndrome associated with two novel compound heterozygous mutations in LRP5.
- Alonso N1, Soares DC, V McCloskey E, Summers GD, Ralston SH, Gregson CL.
- Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.J Bone Miner Res.2015 Apr;30(4):615-20. doi: 10.1002/jbmr.2403.
- Osteoporosis pseudoglioma syndrome (OPPG) is a rare autosomal recessive condition of congenital blindness and severe childhood osteoporosis with skeletal fragility, caused by loss-of-function mutations in the low-density lipoprotein receptor-related protein 5 (LRP5) gene. We report the first case of
- PMID 25384351
Japanese Journal
- 家族性滲出性硝子体網膜症の原因遺伝子の骨密度への影響
- 中森 玄司,近藤 寛之,内尾 英一
- 眼科臨床紀要 = Folia Japonica de ophthalmologica clinica 1(11), 1094-1097, 2008-11-15
- NAID 10023922255
- 目で見るBone Biology(第7回)LRP/Wntと骨代謝
Related Links
- Osteoporosis-pseudoglioma syndrome is a rare condition characterized by severe thinning of the bones (osteoporosis) and eye abnormalities that lead to vision loss. In people with this condition, osteoporosis is usually ...
- Osteoporosis-pseudoglioma syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. ... Osteoporosis-pseudoglioma syndrome: Introduction ...
Related Pictures
★リンクテーブル★
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- 英
- osteoporosis-pseudoglioma syndrome
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