There are only a few reports on supernumerary kidney However, its discovery being difficult in places where diagnostic facilities are not easily accessible. We present a case of A 9 year old girl with a congenital malformation and supernumerary kidney at right upper pole of the right kidney with a mega urethra in which there is pus. The main complaint was a mild, persistent lower abdominal pain associated with virginal reflux. Urine analysis and culture as well as serum blood values were within normal limits. The diagnosis of visceral malformations, particularly a supernumerary kidney is not easy, especially in an environment where diagnostic facilities are not easily accessible.Pan African Medical Journal 2016; 2
Late presentation of symptomatic hydrometrocolpos is uncommon. We present a 5 years old continent gi...
Introduction: The spectrum of congenital anomalies of the kidneys and the urinary tract is extremely...
Hydronephrosis associated with kidney malrotation can be a surgical challenge. We present the case o...
Supernumerary kidney is the rarest of all renal anomalies; fewer than 80 cases have been reported in...
Abstract: Background: A supernumerary kidney (SK) is an additional kidney with its own capsule and b...
Supernumerary kidney (SNK) is a rare congenital anomaly with fewer than 100 cases reported in the En...
AbstractWe report a case of supernumerary kidney consisting of 4 renal moieties and including a hors...
Supernumerary kidney is a one of the rarest congenital renal anomalies with less than 100 cases repo...
The supernumerary kidney especially on right side is a rare diagnosis. Only few case reports are doc...
Congenital anomalies of the kidney and urinary tract are part of a family of diseases with different...
Supernumerary kidneys are very rare renal malformations, little described in the literature. Its dia...
Item does not contain fulltextBACKGROUND: Unilateral renal agenesis (URA) is associated with other c...
Thoracic kidney is a rare type of renal ectopia. Patients with thoracic kidneys are usually asymptom...
Renal segmental hypoplasia (Ask-Upmark kidney) is a congenital disorder, first described by Eric As...
No Abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/38195/1/1870210411_ftp.pd
Late presentation of symptomatic hydrometrocolpos is uncommon. We present a 5 years old continent gi...
Introduction: The spectrum of congenital anomalies of the kidneys and the urinary tract is extremely...
Hydronephrosis associated with kidney malrotation can be a surgical challenge. We present the case o...
Supernumerary kidney is the rarest of all renal anomalies; fewer than 80 cases have been reported in...
Abstract: Background: A supernumerary kidney (SK) is an additional kidney with its own capsule and b...
Supernumerary kidney (SNK) is a rare congenital anomaly with fewer than 100 cases reported in the En...
AbstractWe report a case of supernumerary kidney consisting of 4 renal moieties and including a hors...
Supernumerary kidney is a one of the rarest congenital renal anomalies with less than 100 cases repo...
The supernumerary kidney especially on right side is a rare diagnosis. Only few case reports are doc...
Congenital anomalies of the kidney and urinary tract are part of a family of diseases with different...
Supernumerary kidneys are very rare renal malformations, little described in the literature. Its dia...
Item does not contain fulltextBACKGROUND: Unilateral renal agenesis (URA) is associated with other c...
Thoracic kidney is a rare type of renal ectopia. Patients with thoracic kidneys are usually asymptom...
Renal segmental hypoplasia (Ask-Upmark kidney) is a congenital disorder, first described by Eric As...
No Abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/38195/1/1870210411_ftp.pd
Late presentation of symptomatic hydrometrocolpos is uncommon. We present a 5 years old continent gi...
Introduction: The spectrum of congenital anomalies of the kidneys and the urinary tract is extremely...
Hydronephrosis associated with kidney malrotation can be a surgical challenge. We present the case o...