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遗传性颅骨锁骨发育不全一例

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摘要 颅骨锁骨发育不全为罕见的全身骨骼发育不全疾病,为基因异常导致的可遗传性疾病,本病例为家族遗传性病例,通过描述该病的X线表现,来进行诊断及鉴别诊断。
出处 《罕少疾病杂志》 2014年第3期56-57,共2页 Journal of Rare and Uncommon Diseases
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参考文献6

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二级参考文献5

  • 1Robert M. Freedom. Congenital Heart Disease Textbook of Angiocardiography. Futura Publishing Company, Inc. 975-950.
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  • 4Marinho DA, Silva AJ, et al. True double aortic lumen in tetralogy of Fallot. Int J Cardiol, 1998, 63: 2,117-119.
  • 5Lambert V, Blaysat G, Sidi D, et al. Double-lumen aortic arch by persistence of fifth aortic arch: a new case associated with COA.Pediatr Cardiol,1999, 20: 2,167-169.

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