Results 31 to 40 of about 736,585 (190)

Butterfly adrenal gland with maldevelopment of the mesonephric duct: A rare association in an adult patient

open access: yesRadiology Case Reports, 2018
Adrenal gland disorders can be asymptomatic and detected incidentally via imaging techniques such as ultrasound, computed tomography (CT), positron emission tomography, and magnetic resonance imaging.
Nur Hursoy, MD   +2 more
doaj   +1 more source

Zinner Syndrome

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2021
Zinner syndrome is a developmental anomaly of the urogenital tract. This condition is defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. The syndrome is due to malformation of
Abakar Djidda   +5 more
doaj   +1 more source

Unilateral autosomal dominant polycystic kidney disease with co-existent renal cell carcinoma: A rare entity

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2018
Bilateral ADPKD is a well-known entity, but there are only a few reports on unilateral ADPKD in adults, most of which had associated contralateral agenesis. Further rare is the development of RCC in unilateral ADPKD.
Anupama Tandon   +4 more
doaj   +1 more source

POTTER SYNDROME, A RARE ENTITY WITH HIGH RECURRENCE RISK IN WOMEN WITH RENAL MALFORMATIONS – CASE REPORT AND A REVIEW OF THE LITERATURE [PDF]

open access: yesRomanian Journal of Pediatrics, 2017
Potter syndrome represents an association between a specific phenotype and pulmonary hypoplasia as a result of oligohydramnios that can appear in different pathological conditions.
George Rolea   +4 more
doaj   +1 more source

Obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) syndrome with imperforate anus

open access: yesJournal of Pediatric Surgery Case Reports, 2016
OHVIRA syndrome (Obstructed hemivagina with ipsilateral renal agenesis) is a rare Mullerian duct anomaly that results in uterine didelphys, obstructed vaginal vault, and unilateral renal agenesis.
Peter Cosgrove   +3 more
doaj   +1 more source

Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations

open access: yesUrology Case Reports, 2014
Congenital absence of the vas occurs in up to 1% of men. Congenital unilateral absence of the vas deferens can be related to cystic fibrosis transmembrane conductance regulator mutations or in 79% of cases, renal agenesis.
Gregory Shepherd, Ashok Rajimwale
doaj   +1 more source

HERLYN-WERNER-WUNDERLICH SYNDROME-ROLE OF IMAGING IN TIMELY AND CORRECT DIAGNOSIS

open access: yesPakistan Armed Forces Medical Journal, 2021
We present this case of uterus didelphys with right sided haematometrocolpos due to obstructed hemivagina and ipsilateral renal agenesis-Herlyn Werner Wunderlich syndrome.
Hidayat Ullah   +3 more
doaj   +1 more source

Unilateral Renal Agenesis and the Awareness of Mostyn Embrey Syndrome

open access: yes, 2017
Al-Mosawi AJ. Unilateral Renal Agenesis and the Awareness of Mostyn Embrey Syndrome. Journal of Renal Medicine 2017; 1(1):1-4. Published: March 21, 2017.
Al-Mosawi,Aamir
core   +1 more source

Unilateral renal agenesis: three case reports

open access: yes, 2017
Unilateral renal agenesis (incidence of 1/500–1000 newborns), can be isolated or associated with other urological/extra-urological abnormalities. Unilateral renal agenesis (URA) may be suspected after a renal US and confirmed by static renal scintigraphy.
PETTOELLO MANTOVANI, MASSIMO   +5 more
core   +1 more source

Retrocaval ureter and contra lateral renal agenesis – a case report and review of literature

open access: yesInternational Brazilian Journal of Urology
Associated congenital anomalies are seen in 21% of retrocaval ureter patients; among them, associated contralateral renal agenesis is a very rare entity.
Felix Cardoza   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy