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鱼鳞病伴发僵人综合征2例

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出处 《疑难病杂志》 CAS 2009年第2期117-117,共1页 Chinese Journal of Difficult and Complicated Cases
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  • 1[1]Stoll C, Eyer D. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy. Ann Genet, 1999,42:45
  • 2[2]Kaufman LM. A syndrome of retinitis pigmentosa, congenital ichthyosis, hypergonadotropic hypogonadism, small stature, mental retardation, cranial dysmorphism, and abnormal electroencephalogram. Ophthalmic Genet, 1998,19:69
  • 3[3]Tercedor J, Garcia A. Keratotic neurocutaneous syndromes. Rev Neurol, 1997,25:S238
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  • 5[5]Gohlke BC, Haug K, Fukami M, et al. Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. J Med Genet, 2000,37:600
  • 6Rand RE,Baden HP.The ichthyosis:a review[J].J Am Acad Dermatol,1983,8(3):285-305.
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  • 10王维治.中枢神经系统脱髓鞘疾病.见:王维治主编.神经病学.第4版.北京:人民卫生出版社,2002.191

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