Abstract
We report the US and MR appearances in a case of persistent Müllerian duct syndrome, a rare form of inherited male pseudohermaphroditism characterised by the presence of uterus and fallopian tubes in a normally virilised 46XY male.
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Received: 23 May 1997 Accepted: 21 January 1998
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Di Cesare, E., Di Bartolo De Vincentiis, V., Maffey, M. et al. US and MRI in a case of persistent Müllerian duct syndrome. Pediatric Radiology 28, 865–867 (1998). https://doi.org/10.1007/s002470050484
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DOI: https://doi.org/10.1007/s002470050484