MULLERIAN ANOMALY AND FEMALE HYPOSPADIAS-A RARE CASE REPORT
Abstract
Mullerian Duct Anomalies occur in 2-3 of
all women.Congenital anomalies of female
genital tract results from mullerian
duct anomalies and abnormalities of cloaca
and urogenital sinus. Associated urinary
tract anomalies are common due to
the close developmental relationship between
the two. Here we present a case
of female hypospadias and mullerian
duct anomaly.A 24 year old G3P2L0 with
previous two caesarean section with Bicornuate
uterus with pregnancy in left
horn was admitted and she was managed
by elective repeat caesarean section.
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