MULLERIAN ANOMALY AND FEMALE HYPOSPADIAS-A RARE CASE REPORT
Journal: University Journal of Surgery and Surgical Specialities (Vol.3, No. 1)Publication Date: 2017-02-09
Authors : KARTHIHA;
Page : 13-15
Keywords : :Female Hypospadias; Bicornuate uterus;
- A CASE OF ABRUPTION TAKEN UNAWARE
- A RARE CASE OF ABRUPTION WITH LUTEOMA OF PREGNANCY
- TRAUMATIC PLACENTAL ABRUPTION AND SPLENIC RUPTURE IN PREGNANCY- a case report
- A clinical case of successful treatment of complete abruption of the trachea from the larynx
- Large Prostatic Calculus in an Alkaptonuria patient – Caught unaware
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.
Other Latest Articles
Last modified: 2017-02-27 15:41:58