潜在性二分頭蓋
WordNet
- hide from view; "The lids were occulting her eyes"
- supernatural practices and techniques; "he is a student of the occult" (同)occult arts
- become concealed or hidden from view or have its light extinguished; "The beam of light occults every so often"
- hidden and difficult to see; "an occult fracture"; "occult blood in the stool"
- the part of the skull that encloses the brain (同)braincase, brainpan
- divided into two lobes; "a bifid petal"
PrepTutorEJDIC
- 秘法の / 人間の理解を越えた,神秘の / 超自然の世界
- 頭蓋
UpToDate Contents
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English Journal
- A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies.
- Labonne JD1,2, Vogt J3, Reali L3, Kong IK4, Layman LC1,2,5, Kim HG1,2.
- American journal of medical genetics. Part A.Am J Med Genet A.2015 Dec;167(12):3011-8. doi: 10.1002/ajmg.a.37344. Epub 2015 Sep 3.
- In Potocki-Shaffer syndrome (PSS), the full phenotypic spectrum is manifested when deletions are at least 2.1 Mb in size at 11p11.2. The PSS-associated genes EXT2 and ALX4, together with PHF21A, all map to this region flanked by markers D11S1393 and D11S1319. Being proximal to EXT2 and ALX4, a 1.1
- PMID 26333423
- MSX2 Gene Duplication in a Patient with Eye Development Defects.
- Plaisancié J1, Collet C2, Pelletier V1, Perdomo Y1, Studer F1, Fradin M3, Schaefer E3, Speeg-Schatz C4, Bloch-Zupan A5, Flori E6, Dollfus H1,3,7.
- Ophthalmic genetics.Ophthalmic Genet.2015 Dec;36(4):353-8. doi: 10.3109/13816810.2014.886270. Epub 2014 Mar 25.
- BACKGROUND: MSX2 mutations are a very rare cause of craniosynostosis. Gain-of-function mutations may lead to the Boston-type craniosynostosis with limb defects and refraction errors, whereas loss-of-function mutations causes primary osseous defects such as enlarged parietal foramina.MATERIALS AND ME
- PMID 24666290
- The extracranial to intracranial anastomotic channel through the parietal foramen: delineation with magnetic resonance imaging.
- Tsutsumi S1, Nonaka S2, Ono H3, Yasumoto Y2.
- Surgical and radiologic anatomy : SRA.Surg Radiol Anat.2015 Oct 24. [Epub ahead of print]
- PURPOSE: Parietal foramina (PFs) are openings of fine canals that perforate the parietal bone. However, few studies have investigated the entire canals and their emissary vessels (EVs). Here, we explore the EVs with magnetic resonance imaging.METHODS: A total of 104 patients who underwent contrast e
- PMID 26498934
Related Links
- (Cranium bifidum occultum) (Cranium bifidum, hereditary) (Parietal foramina 1; PFM1, included) 頭頂孔 (頭頂孔, 対称性) (永久頭頂孔;) (Catlin マーク) (潜在性二分頭蓋) (二分頭蓋, 遺伝性) (頭頂孔1) 責任遺伝子:123101 Muscle ...
- 1. Am J Orthod Dentofacial Orthop. 2006 Jun;129(6):825-8. Hereditary cranium bifidum persisting as enlarged parietal foramina (Catlin marks) on cephalometric radiographs. Mupparapu M(1), Binder RE, Duarte F. Author ...
★リンクテーブル★
[★]
- ラ
- cranium bifidum occultum
[★]
- 関
- cryptic、initiated、latency、latent、subclinical
[★]
- 関
- bipartite、bisect、bisection、dichotic、dichotomous