Results 21 to 30 of about 1,510 (167)

Female Epispadias: A Case Report and Review of the Literature

open access: yesKaohsiung Journal of Medical Sciences, 2009
Isolated female epispadias without exstrophy is an extremely rare syndrome. The symptoms of female epispadias are primary urinary incontinence and abnormal anatomical features. A 12-year-old girl presented with primary urinary incontinence.
Dogan Atilgan   +3 more
doaj   +1 more source

Epispadias and Exstrophy [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1969
Exstrophy of the bladder is the commonest member of a group of anomalies of varying severity in which there is a failure of symphysis of the pubic bones, a defect of the abdominal wall, a deficiency of the ventral aspect of the genitourinary tract and sometimes anomalies of the lower bowel.
openaire   +2 more sources

A duplicated Urethra with epispadias: An uncommon association

open access: yesUrology Case Reports, 2023
Epispadias is a malformation of the urethra in which the urethral opening ends on the dorsum of the penis. It is considered a rare anomaly, especially when associated with urethral duplication.
Sahar AlJumaiah   +2 more
doaj   +1 more source

Epispadias with complete prepuce: A rare anomaly

open access: yesAfrican Journal of Urology, 2012
Epispadias with complete prepuce is a very rare anomaly. It is often associated with late presentation because it is a very rare condition and the penis appears grossly normal, thus, the diagnosis is easily missed during the neonatal period.
H.Y. Maitama   +3 more
doaj   +1 more source

Modified Cantwell–Ransley repair for isolated continent epispadias in adult: Our experience

open access: yesIndian Journal of Plastic Surgery, 2017
Purpose: We evaluate here our experience with modified Cantwell–Ransley technique described by Gearhart for correction of isolated continent epispadias in adults with respect to its long-term functional outcome and complications.
Venkat Arjunrao Gite   +3 more
doaj   +1 more source

Bladder exstrophy in adulthood

open access: yesIndian Journal of Urology, 2008
Background: We report our experience with the treatment of classic exstrophy of the bladder in a small series of seven adult males. There are very few documented cases of adults presenting with exstrophy of bladder in literature.
R B Nerli   +5 more
doaj   +1 more source

Exstrophy epispadias complex- Issues beyond the initial repair

open access: yesIndian Journal of Urology, 2012
Despite advances in the management of exstrophy epispadias complex (EEC), the quality of life of these patients is far from good. The post-operative period is complicated by numerous and variable events - infection, dehiscence, upper tract dilatation ...
Jai K Mahajan, Kattragadda L.N. Rao
doaj   +1 more source

Essential embryology for the Canadian pathologists’ assistant

open access: yesAnatomical Sciences Education, Volume 19, Issue 7, Page 1134-1156, July 2026.
Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci   +4 more
wiley   +1 more source

The Exstrophy-epispadias complex [PDF]

open access: yesOrphanet Journal of Rare Diseases, 2009
Exstrophy-epispadias complex (EEC) represents a spectrum of genitourinary malformations ranging in severity from epispadias (E) to classical bladder exstrophy (CEB) and exstrophy of the cloaca (EC). Depending on severity, EEC may involve the urinary system, musculoskeletal system, pelvis, pelvic floor, abdominal wall, genitalia, and sometimes the spine
Reutter Heiko   +3 more
openaire   +3 more sources

Homozygous Loss‐of‐Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities

open access: yesClinical Genetics, Volume 110, Issue 1, Page 64-72, July 2026.
Biallelic SLC20A1 loss‐of‐function variant causes a previously unrecognized multisystem developmental disorder. We report the first homozygous case presenting with tetralogy of Fallot, renal agenesis, polydactyly, and growth impairment. Transcriptome analysis of patient‐derived fibroblasts suggests significant dysregulation of pathways critical for ...
Eugénie Koumakis   +9 more
wiley   +1 more source

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