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Publication : The persistent Müllerian duct syndrome: a molecular approach.

First Author  Guerrier D Year  1989
Journal  J Clin Endocrinol Metab Volume  68
Issue  1 Pages  46-52
PubMed ID  2562843 Mgi Jnum  J:48607
Mgi Id  MGI:1276045 Doi  10.1210/jcem-68-1-46
Citation  Guerrier D, et al. (1989) The persistent Mullerian duct syndrome: a molecular approach. J Clin Endocrinol Metab 68(1):46-52
abstractText  A rare form of male pseudohermaphroditism is characterized by the persistence of Mullerian derivatives in phenotypic males. To determine the etiology of this syndrome, we studied the expression of anti-Mullerian hormone (AMH) in six boys, including three brothers, with the persistent Mullerian duct syndrome. All except one presented with an inguinal hernia containing the Mullerian derivatives, and in two boys the hernial sac contained the contralateral testis. AMH was normally expressed in the testicular tissue of two patients, as shown by bioassay of anti-Mullerian activity and immunocytochemistry. The testicular tissue of the other patients had no detectable bioactive or immunoreactive AMH, yet they expressed AMH mRNA with a normal transcription initiation site and in the amount expected for their age. These results prove the heterogeneity of the persistent Mullerian duct syndrome and suggest that it may sometimes involve peripheral insensitivity to AMH.
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