Results 41 to 50 of about 3,659 (225)
Clinical Genetics, EarlyView.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
Intensive medical student involvement in short-term surgical trips provides safe and effective patient care: a case review [PDF]
, 2011 Background The hierarchical nature of medical education has been thought necessary for the safe care of patients. In this setting, medical students in particular have limited opportunities for experiential learning.
Ira L Leeds +6 more
core +1 more source
Gastric signet‐ring cell carcinoma in a child: A clinical case study
JPGN Reports, Volume 7, Issue 2, Page 285-288, May 2026.Abstract Gastric signet‐ring cell carcinoma (SRCC) is a rare form of gastric cancer characterized by mucus‐rich tumor cells forming a distinctive ring‐like appearance and is exceedingly rare in children, accounting for less than 1% of all childhood malignancies.
Jiaxian Wang +6 more
wiley +1 more source
Developing sustainable Emergency Urology Simulation Training in sub‐Saharan Africa
BJUI Compass, Volume 7, Issue 3, March 2026.Abstract Background Simulation‐based education (SBE) is widely adopted in high‐income countries to enhance surgical training, but opportunities remain limited in low‐ and middle‐income countries (LMICs). Emergency Urology Simulation Training (EUST) was developed to address knowledge and skill gaps in managing urological emergencies in sub‐Saharan ...
William James Gladstone Finch +11 more
wiley +1 more source
Risk of cryptorchidism among sons of horticultural workers and farmers in Denmark
Scandinavian Journal of Work, Environment & Health, 2014 OBJECTIVES: Previous studies indicate an increased risk of cryptorchidism, incomplete testicular descent, among sons of women working with pesticides. This study assessed the risk of cryptorchidism among boys of parents employed as horticultural workers ...
Kristian Tore Jørgensen +5 more
doaj +1 more source
Undescended testis: 513 patients’ characteristics, age at orchidopexy and patterns of referral [PDF]
, 2013 10.1136/archdischild-2013-305225Archives of Disease in Childhood995401 ...
Allen Jr., John Carson +8 more
core +1 more source
Urology Annals, 2013 Background/Purpose : To assess the outcome of the primary laparoscopy-assisted orchiopexy (LAO) and the laparoscopic two-stage Fowler Stephens orchiopexy (FSO) for managing patients with nonpalpable testis in terms of safety, feasibility and efficacy ...
Abdulrahman Alzahem
doaj +1 more source
Transverse testicular ectopia with fused vas deferens
Journal of Pediatric Surgery Case Reports, 2021 Transverse testicular ectopia (TTE) is a rare congenital anomaly where both testicles are migrated in the same hemiscrotum or inguinal canal. The etiology is unknown and it has three types.
Turyalai Hakimi +3 more
doaj +1 more source
AMHR2 mutation in persistent Müllerian duct syndrome: A case of transverse testicular ectopia
UroPrecision, Volume 4, Issue 1, Page 64-68, March 2026.Abstract Backgroud Persistent Müllerian duct syndrome (PMDS) is a rare condition characterized by the persistence of Müllerian duct structures in genotypic and phenotypic males. Case Presentation We present the case of a 4‐month‐old male with PMDS who presented with transverse testicular ectopia. The patient underwent diagnostic laparoscopic orchiopexy
Hangcheng Fu +2 more
wiley +1 more source
Research and Reports in Urology, 2020 Shunta Hori, Katsuya Aoki, Nobutaka Nishimura, Yosuke Morizawa, Daisuke Gotoh, Shinji Fukui, Yasushi Nakai, Makito Miyake, Kazumasa Torimoto, Kiyohide Fujimoto Department of Urology, Nara Medical University, Kashihara, Nara 634-8522, JapanCorrespondence:
Hori S +9 more
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