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Persistence of müllerian duct derivative syndrome in 2 male patients with bilateral cryptorchidism.

Abstract
The persistent müllerian duct syndrome represents a rare form of male pseudohermaphroditism secondary to anti-müllerian hormone deficiency. We describe 2 cases of phenotypically male postpubertal patients with a uterus and tubes. Both patients presented with bilateral cryptorchidism, 1 was seen for gynecomastia and 1 was seen for an abdominal mass that was found to be a testicular tumor.
AuthorsC A Souto, M da C Oliveira, C Telöken, G Paskulin, K Hoffmann
JournalThe Journal of urology (J Urol) Vol. 153 Issue 5 Pg. 1637-8 (May 1995) ISSN: 0022-5347 [Print] United States
PMID7714994 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Glycoproteins
  • Growth Inhibitors
  • Testicular Hormones
  • Anti-Mullerian Hormone
Topics
  • Adolescent
  • Adult
  • Anti-Mullerian Hormone
  • Cryptorchidism (complications)
  • Disorders of Sex Development (complications, diagnosis, genetics)
  • Glycoproteins
  • Growth Inhibitors (deficiency)
  • Gynecomastia (complications)
  • Humans
  • Male
  • Mullerian Ducts
  • Seminoma (complications)
  • Testicular Hormones (deficiency)
  • Testicular Neoplasms (complications)

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