- 同
- 頭蓋裂孔
English Journal
- The efficacy of custom-made porous hydroxyapatite prostheses for cranioplasty: evaluation of postmarketing data on 2697 patients.
- Stefini R1, Zanotti B, Nataloni A, Martinetti R, Scafuto M, Colasurdo M, Tampieri A.
- Journal of applied biomaterials & functional materials.J Appl Biomater Funct Mater.2014 Dec 19:0. doi: 10.5301/jabfm.5000211. [Epub ahead of print]
- PURPOSE: Cranioplasty is a surgical intervention aimed at reestablishing the integrity of skull defects. Autologous bone is still considered the treatment of choice for cranioplasty. The aims of this study were to characterize and evaluate the efficacy of porous hydroxyapatite (HA) to fill skull def
- PMID 25589160
- Use of "custom made" porous hydroxyapatite implants for cranioplasty: postoperative analysis of complications in 1549 patients.
- Stefini R1, Esposito G, Zanotti B, Iaccarino C, Fontanella MM, Servadei F.
- Surgical neurology international.Surg Neurol Int.2013;4:12. doi: 10.4103/2152-7806.106290. Epub 2013 Jan 28.
- BACKGROUND: Cranioplasty is a surgical intervention aimed at reestablishing the integrity of skull defects, and should be considered the conclusion of a surgical act that began with bone flap removal. Autologous bone is still considered the treatment of choice for cranioplasty. An alternative choice
- PMID 23493459
- Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
- Vásquez-Velásquez AI1, García-Castillo HA, González-Mercado MG, Dávalos IP, Raca G, Xu X, Dwyer E, Rivera H.
- Cytogenetic and genome research.Cytogenet Genome Res.2011;132(4):233-8. doi: 10.1159/000321647. Epub 2010 Nov 10.
- We report on 2 similarly affected cousins with a compound imbalance resulting from a familial t(5;9)(q34;p23) and entailing both an ∼17-Mb 5q terminal duplication and an ∼12-Mb 9p terminal deletion as determined by G-banding, subtelomere FISH, and aCGH. The proband's karyotype was 46,XX,der(9)t(
- PMID 21063078
Japanese Journal
- 外傷性くも膜下出血, 脳挫傷, 両側気胸を合併した Craniolacunia の1新生児例
- 吉田 忍,西澤 嘉四郎
- 日本周産期・新生児医学会雑誌 = Journal of Japan Society of Perinatal and Neonatal Medicine 44(3), 742-745, 2008-08-20
- NAID 10023969460
- Large Encephalocele at the Anterior Fontanel : Case Report
- KITANO Ikuo,MATSUMOTO Takashi,TANAKA Yuichi,USHIO Yukitaka,YOKOTA Akira
- Neurologia medico-chirurgica 29(5), 414-416, 1989-05-15
- … A plain skull x-ray revealed craniolacunia and a computed tomography (CT) scan showed maldevelopment of the cerebrum. …
- NAID 110002277893
- Four cases of frontal encephalomeningocele in neonates.
- HAYASHI TAKASHI,KADOWAKI TETSURO,HASHIMOTO TAKEO,SHOJIMA KAZUHITO,UTSUNOMIYA HIDETSUNA,HONDA EIICHRO
- The Kurume Medical Journal 31(1), 27-35, 1984
- … Three cases with craniolacunia were all complicated by congenital hydrocephalus and ventriculoperitoneal shunt was carried out. …
- NAID 130000889368
Related Links
- cra·ni·o·la·cu·ni·a (krā'nē-ō-lă-kū'nē-ă), Incomplete formation of the bones of the vault of the fetal cranium so that there are nonossified areas in the calvaria. Synonym(s): craniofenestria [cranio- + L. lacuna, cleft] craniolacunia /cra·nio ...
- craniolacunia・Luecken Shadel ともいう。 骨の異形成であり、脳圧亢進や水頭症とは無関係。生後6ヶ月以内に消失する。キアリ奇形 type IIに合併しやすい。この場合も脳圧亢進や水頭症とは無関係。 convolutional marking とは似ている ...
Related Pictures
★リンクテーブル★
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- 英
- craniolacunia
- 同
- 裂孔頭蓋 lacunar skull