scholarly journals Living-related kidney transplantation with catheterizable urinary conduit in prune belly syndrome: A case report

2018 ◽  
Vol 51 ◽  
pp. 150-153 ◽  
Author(s):  
Taro Banno ◽  
Yoichi Kakuta ◽  
Kohei Unagami ◽  
Akiko Sakoda ◽  
Masayoshi Okumi ◽  
...  
2019 ◽  
Vol 6 (6) ◽  
pp. 331-334
Author(s):  
Muoneke Vivian Uzoamaka ◽  
Nwokoye Ikenna ◽  
Ezeanosike Obumneme ◽  
Onyire Nnamdi Benson ◽  
Nwokeji-Onwe Linda ◽  
...  

2015 ◽  
Vol 23 (3) ◽  
pp. 215-219
Author(s):  
Tuğçe BARÇA ŞEKER ◽  
Ayşe Çiğdem TÜTÜNCÜ

2008 ◽  
Vol 2 (1) ◽  
Author(s):  
Kotb A Metwalley ◽  
Hekma S Farghalley ◽  
Alaa A Abd-Elsayed

Author(s):  
Shivya Parashar ◽  
Rajesh Malik ◽  
Radha S. Gupta ◽  
Kamaljeet S. Randhawa

1981 ◽  
Vol 146 (10) ◽  
pp. 717-718
Author(s):  
Arthur C. Wittich ◽  
Charles R. Cochrane ◽  
Jenny E. Brockdorff

1974 ◽  
Vol 46 (11) ◽  
pp. 897-899 ◽  
Author(s):  
AGOP KARAMANIAN ◽  
RICHARD KRAVATH ◽  
HIDEO NAGASHIMA ◽  
HANS-HEINRICH GENTSCH

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Azhar Farooqui ◽  
Alaa AlAqeel ◽  
Zakaria Habib

Prune belly syndrome (PBS) is a rare congenital anomaly characterized in males by a triad of anomalous genitourinary tract, deficient development of abdominal wall muscles, and bilateral cryptorchidism. Although similar anomalies have been reported in females, by definition they do not full fill the classical triad. Urorectal septum malformation sequence (URSM) is a lethal condition characterized by presence of ambiguous genitalia, absent perineal openings (urogenital and anal), and lumbosacral abnormalities. In this original case report, the authors discuss the presentation and management of what would be analogous to a Woodhouse category 1 PBS in a female newborn associated with an overlapping presentation of URSM.


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