Results 81 to 90 of about 736,585 (190)

Renal agenesis [PDF]

, 2012
Renal agenesis is relatively common, genetically determined, disease. Genes which lead to its origin are still unconfirmed. Subject of this study was to perform molecular-genetic analyses of two genes, which are candidate for origin of renal agenesis in ...
Svobodová, Iveta
core   +1 more source

Herlyn-Werner-Wunderlich syndrome in a young female presenting with dysmenorrhea: A case report

Radiology Case Reports
Herlyn-Werner-Wunderlich (HWW) syndrome, popularly known by acronym of obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) is a rare Müllerian and Wolffian duct anomaly.
Prajwal Dahal, MD, Ongden Yonjen Tamang, MD, Rudra Prasad Upadhyaya, MD, Kapil Dawadi, MD, Prajina Pradhan, MD, Sabina Parajuli, MBBS   +5 more
doaj   +1 more source

Kallmann's syndrome with unilateral renal agenesis : a case report

, 1986
CITATION: Honiball, S. & Sandler, M. 1986. Kallmann's syndrome with unilateral renal agenesis : a case report. South African Medical Journal, 70:489-491.The original publication is available at http://www.samj.org.zaA case of Kallmann's syndrome ...
Honiball, S., Sandler, M.
core  

Polycystic Kidney Disease Accompanied by Unilateral Renal Agenesis and Ulcerative Colitis: Case Report

, 2012
Autosomal dominant polycystic kidney disease (ODPKD) is characterized by presence of multiple cysts in kidneys and other organs, and it is the most common hereditary kidney disorder.
Dikici, Suleyman, Akinci, Hakan, Erdincler, Deniz Suna, Cengiz, Mahir, Curgunlu, Asli, Doventas, Alper, Yildirim, Erkan   +6 more
core   +1 more source

Zinner syndrome unveiled: Ectopic ureter and seminal vesicle cyst leading to urinary dysfunction: A case report

Radiology Case Reports
Zinner syndrome (ZS) is a rare congenital urological condition characterized by a triad of ipsilateral seminal vesicle cysts, unilateral renal agenesis, and ejaculatory duct obstruction, first described in 1914.
Zaid Sawaftah, Khaled Sawafta, Moath Hattab, Adel Abu Al Rub, Omar Sawafta, Jehad Khamaysa, Humam Emad Rajha, Jana Dibas, Muath Daraghmeh, Yazan Dibas   +9 more
doaj   +1 more source

Clinical characteristics and follow-up results of unilateral renal agenesis and hypoplasia of children

, 2016
Objective: Children with an inadequate number of nephrons have an increased risk of developing hypertension, proteinuria and chronic kidney disease in later life. This renal injury is caused by glomerular hyperfiltration.
Serdaroglu, E, Erkin Serdaroğlu, Selçuk Yüksel, Yüksel, Selçuk, Havva Evrengül, Pelin Ertan, Evrengül, Havva, Ertan, P   +7 more
core   +1 more source

Zinner syndrome: Case report and brief review of the literature

Radiology Case Reports
Zinner syndrome (ZS) is a rare congenital anomaly of the mesonephric (Wolffian) duct, classically defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction.
Kyle R. Knutsen, BS, Rita Sico, D.O., Eyassu Hailemichael, M.D., Cara Lombard, M.D., Dhairya A. Lakhani, M.D.   +4 more
doaj   +1 more source

Unilateral renal agenesis and ipsilateral cryptorchidism : case report

, 2015
A agenesia renal é uma afecção congênita rara na espécie felina, frequentemente associada a uma malformação reprodutiva. O presente trabalho relata o caso de um felino com agenesia renal unilateral associada a criptorquidismo ipsilateral, com ênfase no ...
Santos, Eduardo Rosa dos, Contesini, Emerson Antônio, Rosa, N.S., Oliveira, M.P., Camargo, V.M.F., Barni, Brunna de Souza   +5 more
core   +1 more source

Unilateral renal agenesis, blind-ended ureter, and ectopic ureterocele inserting into the seminal vesicle: A very rare developmental association. [PDF]

Urol Case Rep, 2023
Sorour S, Ferguson C, Wilson MP, Low G.
europepmc   +1 more source

47,XXY with Associated Bilateral Renal Agenesis.

, 2004
We describe the case of a 36-week gestational-age male stillborn with bilateral renal agenesis and a 47,XXY karyotype, as well as features of Potter sequence. No other congenital abnormalities were noted.
Stopyra, Gary A, MD, Barroeta, Julieta E, Stopyra, Gary A   +2 more
core   +1 more source