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http://dx.doi.org/10.4103/jiaps.jiaps_106_23 | DOI Listing |
J Clin Ultrasound
December 2024
NSCB Government Medical College, Jabalpur, India.
Pediatr Surg Int
July 2024
Research Team for the Establishment of Treatment Guidelines for Persistent Cloaca, Cloacal Exstrophy and Mayer-Rokitansky-Küster-Häuser Syndrome for the Proper Transitional Care of the Patients, The Research Project for Rare and Intractable Diseases, Ministry of Health, Labour and Welfare (MHLW), Tokyo, Japan.
Purpose: We investigated the postoperative renal function in persistent cloaca (PC) patients who underwent posterior sagittal anorecto-urethro-vaginopalsty (PSARUVP) and factors influencing the renal functional outcomes.
Methods: A questionnaire survey was distributed to 244 university and children's hospitals across Japan. Of the 169 patients underwent PSARUVP, 103 patients were enrolled in the present study.
Matern Health Neonatol Perinatol
May 2024
Department of Pediatrics, University Hospital Brno, Cernopolni 9, 613 00, Brno, Czech Republic.
J Indian Assoc Pediatr Surg
January 2024
Department of Pediatric Surgery, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
Radiographics
January 2024
From the Department of Radiology and Imaging Sciences, University of Utah Health, 30 N Mario Capecchi Dr, 2nd Floor South, Salt Lake City, UT 84112.
Fetal genitourinary anomalies can present a diagnostic challenge for the radiologist. The absence of a normally located kidney may represent agenesis or be secondary to a fusion or migration abnormality. A dilated renal pelvis should prompt evaluation for a specific cause, including ureteropelvic junction obstruction, reflux, or an obstructed duplicated system.
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