Kondapavuluri SK

No ORCID on file · 1 paper in corpus
case-report 2016
Polish journal of radiology ·doi:10.12659/PJR.897228

BACKGROUND: HWW syndrome is a very rare congenital anomaly of urogenital tract involving Mullerian ducts and mesonephric ducts. It is characterised by a triad of symptoms - uterus didelphys, obstructed hemivagina and ipsilateral renal agene…