Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1111/jpc.15936 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Association between serum albumin and body water using a bioelectrical impedance analyzer: a case report of longitudinal variation in a child with initial idiopathic nephrotic syndrome.
AME Case Rep
May 2024
Department of Pediatrics, Teikyo University School of Medicine, Tokyo, Japan.
Article Synopsis
- - Bioelectrical impedance analysis (BIA) is a noninvasive method for assessing body composition and fluid status, particularly useful in pediatric patients with nephrotic syndrome, where albumin leaks into urine disrupt blood volume.
- - A case study of a 6-year-old with nephrotic syndrome showed a significant negative correlation between serum albumin levels and the extracellular water/total body water ratio (r=-0.72, P<0.04) during treatment with prednisolone.
- - The findings suggest that BIA could reliably predict serum albumin levels noninvasively, potentially minimizing the need for frequent blood tests in children, though further research is necessary for validation.
The First Pediatric Case of an IFT140 Heterozygous Deletion Causing Autosomal Dominant Polycystic Kidney Disease: Case Report.
Case Rep Nephrol Dial
July 2024
Department of Clinical and Molecular Pathology and Medical Genetics, University Hospital Ostrava and Medical Faculty of the University Ostrava, Ostrava, Czech Republic.
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, which is mainly caused by pathogenic variants in two particular genes: and . ADPKD caused by variants in other genes ( or ) is very rare.
Case Report: In a 6-year-old girl examined for abdominal pain, a cystic mass in the upper part of the right kidney was detected during an abdominal ultrasound.
A case of haemoglobinuria in a cat after near-drowning.
Vet Med Sci
July 2024
Animal Emergency Service, Tanawha, Queensland, Australia.
The aim of this study is to describe a case of haemoglobinuria in a cat after near-drowning. A 6-year-old male neutered domestic short hair cat weighing 6.5 kg with a pre-existing seizure disorder presented to an emergency hospital after near-drowning in a swimming pool during a seizure episode.
View Article and Find Full Text PDFIgA nephropathy in a child with X-linked agammaglobulinemia: a case report.
BMC Pediatr
April 2024
Department of Nephrology and Immunology, Qingdao Women and Children's Hospital, Qingdao, China.
Background: X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disease caused by mutations in the Bruton tyrosine kinase (BTK) gene. Individuals diagnosed with XLA are at an increased risk of developing autoimmune diseases. However, renal involvement are rare in cases of XLA.
View Article and Find Full Text PDFNail-patella syndrome with nephropathy in a de novo LMX1B mutation: triangular lunula of the thumb and lack of finger creases as clues.
Pediatr Nephrol
September 2024
Department of Pediatrics, National Hospital Organization Saitama Hospital, Wako, Saitama, Japan.
Article Synopsis
- * Each person's experience with NPS can differ significantly, making diagnosis challenging, especially since kidney biopsies may not provide clear results.
- * A case study of a 6-year-old girl highlighted that genetic testing revealed her condition despite a kidney biopsy showing nonspecific results, emphasizing the need for awareness about certain physical signs to improve diagnosis and avoid unnecessary procedures.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!