WordNet
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- (病気・身体的欠陥など)生まれつきの,先天的な
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- 1. 幼児および小児における緑内障の概要 overview of glaucoma in infants and children
- 2. ウィルムス腫瘍の症状、診断、および病期分類 presentation diagnosis and staging of wilms tumor
- 3. 先天性の細胞遺伝学的異常 congenital cytogenetic abnormalities
- 4. 微細欠失症候群（1番～11番染色体） microdeletion syndromes chromosomes 1 to 11
- 5. 視神経の先天性および後天性異常 congenital anomalies and acquired abnormalities of the optic nerve
English Journal
- Simultaneous correction of post-traumatic aphakia and aniridia with the use of artificial iris and IOL implantation.
- Forlini C, Forlini M, Cavallini GM.SourceDepartment of Ophthalmology, Santa Maria delle Croci Hospital, Viale V. Randi 5 n. 43, 48121, Ravenna, Italy, forlinic@forlinic.it.
- Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie.Graefes Arch Clin Exp Ophthalmol.2013 Oct;251(10):2493-4. doi: 10.1007/s00417-013-2402-8. Epub 2013 Jun 23.
- PMID 23793912
- Analysis of protein composition and protein expression in the tear fluid of patients with congenital aniridia.
- Ihnatko R, Edén U, Lagali N, Dellby A, Fagerholm P.SourceIntegrative Regenerative Medicine Centre and Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, 581 85 Linköping, Sweden. Electronic address: robert.ihnatko@liu.se.
- Journal of proteomics.J Proteomics.2013 Sep 21. pii: S1874-3919(13)00469-7. doi: 10.1016/j.jprot.2013.09.003. [Epub ahead of print]
- Aniridia is a rare congenital genetic disorder caused by haploinsuffiency of the PAX6 gene, the master gene for development of the eye. The expression of tear proteins in aniridia is unknown. To screen for proteins involved in the aniridia pathophysiology, the tear fluid of patients with diagnosed c
- PMID 24061003
- Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation.
- Perez Y, Gradstein L, Flusser H, Markus B, Cohen I, Langer Y, Marcus M, Lifshitz T, Kadir R, Birk OS.SourceThe Morris Kahn Laboratory of Human Genetics at the National Institute of Biotechnology in the Negev, Ben-Gurion University, Beer-Sheva, Israel.
- European journal of human genetics : EJHG.Eur J Hum Genet.2013 Sep 18. doi: 10.1038/ejhg.2013.212. [Epub ahead of print]
- Foveal hypoplasia, always accompanied by nystagmus, is found as part of the clinical spectrum of various eye disorders such as aniridia, albinism and achromatopsia. However, the molecular basis of isolated autosomal recessive foveal hypoplasia is yet unknown. Individuals of apparently unrelated non
- PMID 24045842
Japanese Journal
- 先天無虹彩の1症例におけるFunctional Vision Score評価 (第69回 日本臨床眼科学会講演集(1))
- 臨床眼科 70(3), 367-372, 2016-03
- NAID 40020748541
- Retinal Detachment with Giant Oral Dialysis in an Eye with Congenital Aniridia
- Japanese journal of ophthalmology 54(1), 105-107, 2010-01-01
- NAID 10027203672
- 大阪医科大学における遮光眼鏡の検討
- 日本視能訓練士協会誌 36, 133-139, 2007
- NAID 130003646114
Related Links
- Congenital aniridia syndrome, also known as Aniridia, is a rare disorder described in the database for rare diseases of the Swedish National Board of Health and Welfare. ... Date of publication: 2014-10-09 Version: 2.0 ICD 10 code
- Aniridia is characterized by complete or partial iris hypoplasia usually (but not always) with associated foveal hypoplasia resulting in reduced visual acuity and nystagmus presenting in early infancy. Frequently associated ocular ...
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★リンクテーブル★
| リンク元 | 「先天性無虹彩症」 |
| 関連記事 | 「congenita」「congenital」「aniridia」 |
「先天性無虹彩症」
「congenita」
- adj.
- (後置するラテン語形容詞)先天性の
- ex.
「congenital」
- adj.
- 生まれつきの、先天的な