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苗勒管永存综合征二例

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摘要 曲勒管永存综合征(PMDS)足一种较为甲见的男性假两性畸形,我院共收治2例患者,现报告如下。
出处 《中华外科杂志》 CAS CSCD 北大核心 2007年第12期863-864,共2页 Chinese Journal of Surgery
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参考文献5

  • 1Sheehan SJ, Tobbia IN, Ismail MA, et al. Persistent mullerian duct syndrome: review and report of 3 cases. Br J Urol,1985,57: 548-551.
  • 2Liza Messika-Zeitoun, Lucile Gouedard, Corinne Belville, et al. Autosomal recessive segregation of a truncating mutation of antiMullerian type Ⅱ receptor in a family affected by the persistent Mullerian duct syndrome contrasts with its dominant negative activity in-vitro. J Clin Endocrinol Metab, 2001, 86:4390-4397.
  • 3Loeff DS, Imbeaud S, Reyes HM, et al. Surgical and genetic aspects of persistent mullerian duct syndrome. J Pediatr Surg, 1994,29:61-65.
  • 4Adamsbaum C, Rolland Y, Josso N,et al. Radiological findings in three cases of persistent mullerian duct syndrome. Pediatr Radiol, 1993, 23:55-56.
  • 5Romero FR, Fucs M, Castro MG, et al. Adenocarcinoma of persistent mullerian duct remnants: case report and differential diagnosis. Urology ,2005,66 : 194-195.

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