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Joubert综合征1例 被引量:2

Joubert syndrome:report of one case
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摘要 病例 男,6岁。因智力运动发育落后,肌张力减低,间断出现双眼发直,喘息样呼吸就诊。体检:四肢肌张力减低,肌力Ⅳ-,步态不稳,巴宾斯基征阳性。影像学检查:CT及MR平扫均显示小脑蚓部发育不良,两侧小脑半球间裂增宽,脑干发育异常.脚间窝加深,小脑上脚延长并加厚.呈“臼齿征”,第四脑室形态异常,上部扩大,呈“蝙蝠翼”状(图1,2)。大脑未见明显异常。结合临床诊断为Joubert综合征。
出处 《中国临床医学影像杂志》 CAS 北大核心 2008年第10期754-754,共1页 Journal of China Clinic Medical Imaging
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参考文献3

  • 1Maria BL, Quisling RG. Rosainz LC, et al. Molar tooth sign in Joubert syndrome: clinical radiologic, and pathologic significance [J]. J Child Neurol, 1999, 14: 368.
  • 2朱珍,帕米尔,朱杰明,钱镔.Joubert综合征的CT和MRI诊断[J].中华放射学杂志,2005,39(12):1256-1259. 被引量:34
  • 3Barkovich AJ. Pediatric Neuroimaging [M]. 3rd ed. New York: Raven. 2000. 354-346.

二级参考文献13

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  • 2van Beek EJ,Majoie CB.Case 25:Joubert syndrome.Radiology,2000,216:379-382.
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  • 8Sener RN.Cerebellar vermian clefts disconnecting the hemispheres:a different entity unassociated with Joubert's syndrome.Comput Med Imaging Graph,1997,21:71-75.
  • 9Barkovich AJ.Pediatric Neuroimaging.3rd ed.New York:Raven,2000.345-346.
  • 10Sener RN.A patient with ectodermal dysplasia,Joubert's syndrome,and brain cysts.Comput Med Imaging Graph,1998,22:349-351.

共引文献33

同被引文献26

  • 1朱珍,帕米尔,朱杰明,钱镔.Joubert综合征的CT和MRI诊断[J].中华放射学杂志,2005,39(12):1256-1259. 被引量:34
  • 2王化,谢晟,肖江喜.Joubert综合征一例[J].中华放射学杂志,2006,40(3):328-329. 被引量:4
  • 3王凡.Joubert综合征的MRI表现及诊断价值[J].华西医学,2007,22(3):480-481. 被引量:6
  • 4Keeler LC, Marsh SE, Leeflang EP, et al. Linkage analysis in families with/oubert syndrome plus oculo-renal involvement indentifies the CORS2 lous on chromosome 11p12-q13.3. Am J Hum Genet,2003,73 (3) :656-662.
  • 5Asian H,Gungorduk K, Yildirim G, et al. Prenatal ultrasonographic features of Joubert syndrome. J Clin Ultrasound,2008,36 (9) :576-580.
  • 6Maria BL,boltshauser E,Palmer SC,et al.Clinical features and revised diagnostic critetia in Joubert syndrome.J Child Neurol,1999,14:583-590.
  • 7Gcgraw P.The molar tooth sign.Radiology,2003,229:671-672.
  • 8Maria BL,Quishing RG,Rosainz LC,et al.Molar tooth sign in Joubert syndrome:clinical,radiologic,and pathologic significance.J Child Neurol,1999,14:368-376.
  • 9Joubert M,Eisenring JJ,Robb JP,et al.Familial agenesis of the cerebellar vermis.A syndrome of episodic hyperpenea,abnormal eye movements,ataxia,and retardation.Neurology,1969,19:813-825.
  • 10Boltshauser E,Isler W.Joubert syndrome:episodic hypepnes abnomal eye movements,retardation and ataxia,associated with dysplasis of the cerebellar vermis.Neuropaediatrie,1977,8:57-60.

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