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Large Renal Calculus in a Patient With Crossed Fused Ectopic Kidney Managed With Percutaneous Nephrolithotomy: A Case Report.
Cureus
November 2024
Urology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Congenital anomalies are not regularly seen in day-to-day practice. Crossed fused renal anomalies are even rarer. A 50-year-old female patient presented with right-sided pain in the abdomen with intermittent episodes of burning micturition.
View Article and Find Full Text PDFFraser syndrome with limb reduction defect: a rare and unique anatomic variation.
Surg Radiol Anat
April 2024
Department of Obstetrics & Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad, India.
Introduction: Fraser syndrome, named after George Fraser, is an autosomal recessive disorder showing a highly variable interfamilial phenotypic variation, with malformations ranging from minor symptoms to lethal anomalies like renal agenesis, incompatible with survival. Limb reduction defects have not been reported to be associated with it.
Case Presentation: A 21-year-old primigravida presented to the antenatal outpatient department with a level two targeted anomaly scan report suggestive of severe oligohydramnios with suspected renal agenesis.
Clinical Manifestations and Outcomes of Budd-Chiari Syndrome in Children: A Single-Centre Study.
Cureus
November 2023
Department of Paediatric Gastroenterology and Hepatology, Pakistan Kidney and Liver Institute, Lahore, PAK.
Article Synopsis
- Budd-Chiari syndrome (BCS) is a rare condition in children that leads to ascites and is influenced by the severity and speed of blood vessel blockage in the liver.
- A study analyzed data from 37 patients under 15, revealing that the majority presented with ascites, and many had liver function abnormalities, with chronic BCS being the most common form.
- Treatment options included anticoagulants, radiological interventions, and liver transplants, while some underlying conditions such as Protein C and S deficiencies were identified in the patients.
Omphalocele, Exstrophy of Cloaca, Imperforate Anus, and Spinal Defects Complex: A Case Report.
JNMA J Nepal Med Assoc
April 2023
Department of Pediatrics Surgery, Kanti Children's Hospital, Maharajgunj, Kathmandu, Nepal.
Unlabelled: Omphalocele, exstrophy of cloaca, imperforate anus, and spinal defects complex is a rare malformation complex that includes omphalocele, cloacal exstrophy, imperforate anus and spinal defects with the incidence of 1 in 200,000 to 400,000 pregnancies and is even rarer in twin gestation. The etiology of this complex is still unclear. Most cases are sporadic.
View Article and Find Full Text PDFPrenatal diagnosis of rare cloacal exstrophy: A case report.
Ann Med Surg (Lond)
September 2022
Fetomaternal Division, Department of Obstetrics and Gynecology, Faculty of Medicine, Padjadjaran University, Hasan Sadikin General Hospital Bandung, Indonesia.
Introduction And Importance: Cloacal Exstrophy (CE) is a rare congenital birth defect. A correct prenatal diagnosis of CE is rarely made, even when congenital abnormalities are suspected on prenatal ultrasound examination.
Case Presentation: We report a case of CE with an abdominal defect about 5.
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