Childhood Kidney Diseases (Child Kidney Dis, ChiKD)

Special Article

June 16, 2022

Management strategies for congenital isolated hydronephrosis and the natural course of the disease

Jiwon Jung, Joo Hoon Lee, Kun Suk Kim, et al.

Child Kidney Dis. 2022;26(1):1-10.

Congenital isolated hydronephrosis encompasses a spectrum of physiologic states that spontaneously resolve and pathologic obstruction that necessitates surgical intervention. Distinguishing patients whose condition will resolve, those who will require stringent...

Review Article

June 23, 2022

BK polyomavirus-associated nephropathy

Yo Han Ahn, Hee Gyung Kang

Child Kidney Dis. 2022;26(1):11-17.

BK polyomavirus (BKPyV) is a ubiquitous virus residing in the kidney tubules and is clinically significant only in immunocompromised patients. In clinical practice, BKPyV is a causative pathogen of BKPyV...

Review Article

June 22, 2022

Renal involvement in pediatric rheumatologic diseases

Seong Heon Kim

Child Kidney Dis. 2022;26(1):18-24.

Pediatric rheumatologic diseases are rare systemic diseases that can involve various organs, including the kidneys. Each rheumatologic disease can exhibit characteristic renal involvement, which requires proper treatment and diagnosis. In...

Review Article

June 16, 2022

Mechanism, clinical consequences, and management of dyslipidemia in children with nephrotic syndrome

Hee Sun Baek

Child Kidney Dis. 2022;26(1):25-30.

Dyslipidemia in nephrotic syndrome (NS) is often characterized by marked increases in the levels of total cholesterol, triglycerides, low-density lipoprotein cholesterol, and other lipoproteins, such as very low-density lipoprotein, intermediate-density...

Review Article

May 27, 2022

Alport syndrome: new advances in the last decade

Ji Hyun Kim

Child Kidney Dis. 2022;26(1):31-39.

Alport syndrome (AS) is a progressive hereditary nephritis that is often accompanied by sensorineural hearing loss and ocular abnormalities. It is inherited in three modes of X-linked (XLAS), autosomal recessive...

Original Article

June 23, 2022

Genetic analysis using whole-exome sequencing in pediatric chronic kidney disease: a single center's experience

Hyeonju Lee, Jeesu Min, Yo Han Ahn, et al.

Child Kidney Dis. 2022;26(1):40-45.

Purpose: Chronic kidney disease (CKD) has various underlying causes in children. Identification of the underlying causes of CKD is important. Genetic causes comprise a significant proportion of pediatric CKD cases. Methods:...

Original Article

June 3, 2022

Delta neutrophil index as a predictor of vesicoureteral reflux in children with febrile urinary tract infection

Jae Eun Kim, Jun Suk Oh, Jung Min Yoon, et al.

Child Kidney Dis. 2022;26(1):46-51.

Purpose: Delta neutrophil index (DNI) indicates immature granulocytes in peripheral blood and has been confirmed to be effective as a prognostic factor for neonatal sepsis. Also, it has been reported...

Original Article

June 16, 2022

Predictors of renal scars in infants with recurrent febrile urinary tract infection: a retrospective, single-center study

Jae Ha Han, Seonkyeong Rhie, Jun Ho Lee

Child Kidney Dis. 2022;26(1):52-57.

Purpose: To determine predictive factors for detecting renal parenchymal damages (RPDs) in infants with recurrent febrile urinary tract infection (fUTI). Methods: From January 2015 to December 2021, 102 infants with recurrent...

Case Report

June 16, 2022

Recurrent hemolytic uremic syndrome caused by DGKE gene mutation: a case report

Baek Sup Shin, Yo Han Ahn, Hee Gyung Kang

Child Kidney Dis. 2022;26(1):58-62.

Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury without any association with preceding diarrhea. Dysregulation of the complement system...

Case Report

June 23, 2022

Idiopathic infantile hypercalcemia with severe nephrocalcinosis, associated with CYP24A1 mutations: a case report

Jeesun Yoo, Hee Gyung Kang, Yo Han Ahn

Child Kidney Dis. 2022;26(1):63-67.

Nephrocalcinosis often occurs in infants and is caused by excessive calcium or vitamin D supplementation, neonatal primary hyperparathyroidism, and genetic disorders. Idiopathic infantile hypercalcemia (IIH), a rare cause of nephrocalcinosis,...

Current Issue: Volume 26(1); Jun 2022

Childhood
Kidney Diseases

Print ISSN: 2384-0242
Online ISSN: 2384-0250

MOST READ (Last two years)

Viewed By 24255	Pediatric Acute Kidney Injury: Focusing on Diagnosis and Management
Viewed By 12610	Management of IgA vasculitis nephritis (Henoch-Schonlein purpura nephritis) in Children
Viewed By 11932	Pediatric Hemodialysis
Viewed By 6045	Infectious and Non-infectious Complications of Peritoneal Dialysis in Children
Viewed By 4214	Coexistence of Central Diabetes Insipidus and Prolonged Cerebral Salt Wasting Syndrome after Brain Tumor Surgery: A Case Report

+more

MOST CITED (2020-2022)

Cited By 2	Pediatric Acute Kidney Injury: Focusing on Diagnosis and Management
Cited By 1	Infectious and Non-infectious Complications of Peritoneal Dialysis in Children
Cited By 1	Association of Neutrophil Gelatinase associated Lipocalin and Leukocyte Differential Count in Children with Febrile Urinary Tract Infections
Cited By 1	Clinical Characteristics and Long-Term Prognosis of Alport Syndrome: A Retrospective Single-Center Study
Cited By 1	Effect of Hypertension on Childhood-onset Systemic Lupus Erythematous in a Tertiary Medical Center in Korea

+more

Manuscript Submission
To submit a manuscript, please visit the Child Kidney Dis e-submission management system at esubmit, read the Instructions for Authors, and log into the Child Kidney Dis e-submission system. For assistance with manuscript submission, please contact: chikd@chikd.org.
Free archive
Anyone may access any past or current articles without logging in.

Editorial Office 240, Gimpohangang 1-ro, Gimpo-si, Gyeonggi-do, 10078, Republic of Korea TEL: +82-10-4391-0788 E-mail: chikd@chikd.org
Copyright© Korean Society of Pediatric Nephrology.