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1. スティーブンス・ジョンソン症候群および中毒性表皮壊死融解症：管理、予後、および長期の後遺症 stevens johnson syndrome and toxic epidermal necrolysis management prognosis and long term sequelae

English Journal

Alobar holoprosencephaly with cyclopia - autopsy-based observations from one medical center.

Swatek J, Szumiło J, Burdan F.Author information Department of Clinical Pathomorphology, Medical University of Lublin, Poland. yarons@wp.plAbstractHoloprosencephaly, a major congenital malformation of the brain, consists in a complete or partial failure of the prosencephalon to divide into separate hemispheres. Alobar holoprosencephaly with cyclopia was analyzed on the basis of autopsy reports performed for hospitals admitting patients from the Lublin Region in Eastern Poland in the period of 20 years (1981-2000). The malformation was found in seven newborns - five girls, one boy and one child with sex not established due to agenesia of the genital organs, all autopsied in the years 1990-1999. According to clinical data, none of the mothers (age 24-39 years) was exposed to any prescribed or over-the-counter (OTC) drugs during pregnancy, but one was exposed to paints in early pregnancy. The proboscis was present in four of seven cases. Six of seven children displayed additional congenital malformations. In two cases intrapancreatic accessory spleen suggesting trisomy 13 was found. Alobar holoprosencephaly with cyclopia is a rare lethal congenital anomaly frequently accompanied by other malformations and characterized by large variations in incidence.
Reproductive toxicology (Elmsford, N.Y.).Reprod Toxicol.2013 Nov;41:80-5. doi: 10.1016/j.reprotox.2013.06.060. Epub 2013 Jun 17.
Holoprosencephaly, a major congenital malformation of the brain, consists in a complete or partial failure of the prosencephalon to divide into separate hemispheres. Alobar holoprosencephaly with cyclopia was analyzed on the basis of autopsy reports performed for hospitals admitting patients from th
PMID 23791929

[Congenital mydriasis as an initial sign of septo-optic dysplasia].

Carrascosa-Romero MC, Ruiz-Cano R, Martínez-López F, Alfaro-Ponce B, Pérez-Pardo A.Author information Sección de Neuropediatría, Complejo Hospitalario Universitario de Albacete, Albacete, España. Electronic address: mccarrascosa@sescam.jccm.es.AbstractSepto-optic dysplasia (SOD)[MIM182230] consisting of a heterogeneous and uncommon condition characterised by the classictriad: optic nerve hypoplasia, abnormalities of pituitary hormone, and defects of thebrain midline (including agenesis of the septum pellucidum and/or the corpus callosum; ithas also been described associated cortical malformations, it was referred to as SOD plus syndrome).We report the first known case in which the initial diagnostic sign of SOD was a bilateralmydriasis as a manifestation ofhypoplasia of both optic nerves, pituitary hypoplasia andcerebral dysgenesis with neuronal migration disorder.We discuss thedifferential diagnosis of congenital mydriasis.
Archivos de la Sociedad Española de Oftalmología.Arch Soc Esp Oftalmol.2013 Oct;88(10):398-402. doi: 10.1016/j.oftal.2012.05.005. Epub 2012 Aug 4.
Septo-optic dysplasia (SOD)[MIM182230] consisting of a heterogeneous and uncommon condition characterised by the classictriad: optic nerve hypoplasia, abnormalities of pituitary hormone, and defects of thebrain midline (including agenesis of the septum pellucidum and/or the corpus callosum; ithas al
PMID 24060304

European college of orthodontics: commission of affiliation and titularisation.

Nicolas S.Author information Parc Valgora, centre Hermès, bâtiment 10, 83160 La Valette du Var, France. orthonicolas@hotmail.frAbstractDate of birth: 15/1/1994; gender: male.
International orthodontics / Collège européen d'orthodontie.Int Orthod.2013 Sep;11(3):345-56. doi: 10.1016/j.ortho.2013.06.001. Epub 2013 Jul 20.
Date of birth: 15/1/1994; gender: male.A PRETREATMENT RECORDS: (18/3/2008; 13 y 10 m).DIAGNOSIS: Skeletal Class II due to mandibular retrognathism. Agenesia of 12 and 22. Deep bite due to upper and lower alveolar retrusion.TREATMENT: Leveling of arches using passive self-ligating .022 ×.028" multib
PMID 23880078

Japanese Journal

山羊の近軸性橈骨半肢3例のX線学的所見(短報)(解剖学)

Corbera J. A.,Pulido M.,Moralis M.,Juste M. C.,Gutierrez C.
The journal of veterinary medical science 64(9), 843-845, s・iii-s・iv, 2002-09-25
半肢は肢の正常構造の一部欠損を特徴とする先天性奇形である.本奇形は,横断性と近軸性半肢に分類され,遺伝的と環境的要因が関与する.本論文では,山羊で見られた近軸性半肢3例の異なる症例(橈骨形成不全,橈骨の遠位骨端欠損と尺骨低形成を伴う異常橈骨)をX線により見つけた.これら異常に関する可能な原因を討議した.
NAID 110003920950

ミンク(Mustela vison)-とくにいわゆるホモの不妊に関する形態学的研究 : I.雄の尿生殖器の肉眼的所見

山下忠幸,三須幹男,山本志郎,寺田弘,石井祥之
帯広畜産大学学術研究報告. 第I部 4(1), 27-"42-2", 1963-12-25
いわゆるホモの不妊の原因を形態学的に明らかにする目的で,東北海道の3ミンク飼育場で蒐集したホモ3種類の合計50個体および対照としての3品種の合計33個体の尿生殖器についてまず肉眼的観察を行ない,次のような成績をえた。1)一側の泌尿器に異常が認められた個体に,同時に同一側の生殖器にも異常が認められたもの(尿生殖器異常群)がNAMRのHomo Sapphire3例中1例(33.3%)およびHomo C …
NAID 110006453013

Agenesia bilateral do trajecto craneano da arteria carotida interna

da SILVA G
Rev Otolaryngol (Sao Paulo) 4, 425, 1936
NAID 10004781203

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