American Society of Pediatric Nephrology

American Society of Pediatric Nephrology The ASPN is an organization of pediatric nephrologists and affiliated health care professionals.

Our primary goals are to promote optimal care for children with kidney disease through advocacy,
education and research; and to disseminate advances in clinical practice and scientific investigation.

Low incidence of profound agranulocytosis after rituximab combined with prolonged low-dose prednisolone in children with...
09/10/2026

Low incidence of profound agranulocytosis after rituximab combined with prolonged low-dose prednisolone in children with complicated nephrotic syndrome


https://buff.ly/RPJtHT8

Home Pediatric Nephrology Article Low incidence of profound agranulocytosis after rituximab combined with prolonged low-dose prednisolone in children with complicated nephrotic syndrome Research Letter Published: 02 September 2026 (2026) Cite this article Save article View saved research Pediatric N...

09/10/2026

Hospitalization Costs of Kidney Transplantation Associated With Induction Therapy Among Pediatric Kidney Transplant Recipients: A North American Pediatric Renal Trials and Collaborative Studies and Pediatric Health Information System Collaborative Study.

https://doi.org/10.1111/petr.70441

Case report: Two variants in SLC34A3 in a patient with X-linked hypophosphatemia: a diagnostic and therapeutic dilemma  ...
09/10/2026

Case report: Two variants in SLC34A3 in a patient with X-linked hypophosphatemia: a diagnostic and therapeutic dilemma


https://buff.ly/CkV2IAW

X-linked hypophosphatemia (XLH) is the most prevalent form of hereditary rickets due to pathogenic variants in the PHEX gene. Since 2018, a treatment with burosumab, which inhibits the activity of fibroblast growth factor 23 (FGF23), has been approved for XLH patients. In contrast, hereditary hypoph...

Training programs for families of children on home peritoneal dialysis: a scoping review   https://buff.ly/EgfcmpG
09/09/2026

Training programs for families of children on home peritoneal dialysis: a scoping review



https://buff.ly/EgfcmpG

Background Peritoneal dialysis (PD) is the preferred home dialysis treatment for children awaiting kidney transplant worldwide. There is significant variance in clinical outcomes across centers, which may be related to PD training for caregivers. This scoping review provides an overview of existing....

Patient-reported ratings of transfer to adult care among young adults with chronic kidney disease   https://buff.ly/jy1z...
09/09/2026

Patient-reported ratings of transfer to adult care among young adults with chronic kidney disease



https://buff.ly/jy1zo11

Background Effective healthcare transitions and transfers of care are crucial for improving long-term health outcomes among adolescents and young adults (AYA) with chronic kidney disease (CKD). Patient-reported outcomes are an important tool to understand patient experience and are underused in CKD....

Can urinary albumin-creatinine ratio be used as a surrogate for protein-creatinine ratio in the diagnosis and management...
09/09/2026

Can urinary albumin-creatinine ratio be used as a surrogate for protein-creatinine ratio in the diagnosis and management of pediatric steroid sensitive nephrotic syndrome?


https://buff.ly/lMAgOy8

Background In pediatric nephrotic syndrome (NS), conventionally, spot urinary protein-creatinine ratio (PCR) is used for diagnosis and to define relapse and remission. This study evaluates whether urine albumin-creatinine ratio (ACR) can reliably predict proteinuria status to manage NS according to....

Case report: “A dicey situation:” asymptomatic hypertensive urgency caused by DICER1 mutation–derived cystic nephroma in...
09/09/2026

Case report: “A dicey situation:” asymptomatic hypertensive urgency caused by DICER1 mutation–derived cystic nephroma in a 12-month-old


https://buff.ly/HlxT0VP

Cystic nephroma (CN) in pediatric patients is a rare, benign, multi-lobular cystic mass often indicative of DICER1 tumor predisposition syndrome. This condition is caused by a germline mutation of the DICER1 gene and requires appropriate follow-up to monitor for other DICER1-associated tumors in the...

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