グレーグ両眼隔離症候群
WordNet
- visible; "be sure of it; give me the ocular proof"- Shakespeare; "a visual presentation"; "a visual image" (同)visual
- of or relating to or resembling the eye; "ocular muscles"; "an ocular organ"; "ocular diseases"; "the optic (or optical) axis of the eye"; "an ocular spot is a pigmented organ or part believed to be sensitive to light" (同)optic, optical, opthalmic
- relating to or using sight; "ocular inspection"; "an optical illusion"; "visual powers"; "visual navigation" (同)optic, optical, visual
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- 《文》目の / 《まれ》視覚の,目で見た / (顕微鏡・望遠鏡などの)接眼レンズ,接眼鏡
- (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
- Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.
- Tanteles GA1, Michaelidou S, Loukianou E, Christophidou-Anastasiadou V, Kleopa KA.
- Clinical dysmorphology.Clin Dysmorphol.2015 Jul;24(3):102-5. doi: 10.1097/MCD.0000000000000074.
- Greig cephalopolysyndactyly syndrome (GCPS) is typically characterized by preaxial or mixed preaxial and postaxial polydactyly with or without syndactyly and craniofacial features including hypertelorism and macrocephaly. Although GLI3 shows considerable pleiotropy, it is the only gene known to caus
- PMID 25714367
- A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.
- Patel R1, Tripathi FM2, Singh SK3, Rani A4, Bhattacharya V5, Ali A6.
- Meta gene.Meta Gene.2014 Nov 25;2:880-7. doi: 10.1016/j.mgene.2014.11.002. eCollection 2014.
- Greig cephalopolysyndactyly (GCPS) syndrome is an autosomal dominant disorder with high penetrance in majority of cases, characterized by a triad of polysyndactyly, macrocephaly and hypertelorism. GCPS is known to be caused by mutations in the transcription factor GLI3 gene (7p13) which results in f
- PMID 25606469
- Frontofacial surgery in children and adolescents: techniques, indications, outcomes.
- Britto JA1, Greig A1, Abela C1, Hearst D1, Dunaway DJ1, Evans RD1.
- Seminars in plastic surgery.Semin Plast Surg.2014 Aug;28(3):121-9. doi: 10.1055/s-0034-1384807.
- The techniques of frontofacial surgery are most valuable in the clinical management of complex craniofacial deformity to achieve a range of functional and aesthetic gains in children from infancy to maturity. A variety of complex craniofacial osteotomies that can be used to separate the orbits from
- PMID 25210505
Related Links
- ocular hypertelorism n. Extreme width between the eyes due to an enlarged sphenoid bone, sometimes associated with other congenital deformities and mental retardation. Also called Greig's syndrome. ocular hypertelorism, a ...
- Greig syndrome (1) Ocular hypertelorism, see there. (2) Greig polysyndactyly-craniofacial dysmorphism syndrome (MIM:175700). oc·u·lar hy·per·tel·or·ism [MIM*145400] increased width between the eyes due to an arrest in ...
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- 英
- Greig ocular hypertelorism syndrome
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- 関
- bulbar、eyeball、eyepiece、globe、optic、vision、visual
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