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Angelman综合征合并非进展性肌阵挛脑病

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摘要 第一次查房主治医师查房,入院第2天.
出处 《中国小儿急救医学》 CAS 2014年第2期119-121,共3页 Chinese Pediatric Emergency Medicine
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参考文献6

  • 1Thomson AK,Glasson EJ,Bittles AH. A long-term populationbased clinical and morbidity profile of Angelman syndrome in Western Australia:1953-2003[J].Disabil Rehabi1,2006,(5):299-305.
  • 2Williams CA,Beaudet AL,Clayton-Smith J. Angelman syndrome 2005:updated consensus for diagnostic criteria[J].{H}American Journal of Medicdl Genetics,2006,(5):413-418.
  • 3Minassian BA,DeLorey TM,Olsen RW. Angelman Syndrome:correlations between epilepsy phenotypes and genotypes[J].{H}Annals of Neurology,1998,(4):485-493.
  • 4Varela MC,Kok F,Otto PA. Phenotypic variability in Angelman syndrome:Comparison among different deletion classes and between deletion and UPD subjects[J].{H}European Journal of Human Genetics,2004,(12):987-992.
  • 5Elia M. Myoclonic status in nonprogressive envephalopathies:an Update[J].{H}EPILEPSIA,2009,(z5):41-44.
  • 6Evangeliou A,Doulioglou V,Haidopoulou K. Ketogenic diet in a patient with Angelman syndrome[J].{H}Pediatrics International,2010,(5):831-834.

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