- Anemia in children with chronic kidney disease
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Park MJ, Cho MH
- KMID: 2549738
- Child Kidney Dis.
- 2023 Dec;27(2):82-88.
- doi: 10.3339/ckd.23.016
Chronic kidney disease (CKD) causes numerous changes that destabilize homeostasis, of which anemia is one of its important complications. Anemia significantly reduces the quality of life in children with CKD... -
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- Comprehensive review of membranoproliferative glomerulonephritis: spotlighting the latest advances in revised classification and treatment
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Kim JY
- KMID: 2549735
- Child Kidney Dis.
- 2023 Dec;27(2):64-69.
- doi: 10.3339/ckd.23.015
Membranoproliferative glomerulonephritis (MPGN) is a complex group of renal diseases characterized by a specific pattern of glomerular injury that includes thickening of the capillary wall and mesangial expansion, leading to... -
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- Introducing the general management of glomerular disease from a pediatric perspective based on the updated KDIGO guidelines
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Lim SH
- KMID: 2549734
- Child Kidney Dis.
- 2023 Dec;27(2):55-63.
- doi: 10.3339/ckd.23.009
In 2021, a new chapter on the general management of glomerulonephritis (GN) was added to the Kidney Disease: Improving Global Outcomes (KDIGO). It emphasizes the importance of early general management... -
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- An overview of Dent disease
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Yang EM, Chang SH
- KMID: 2549736
- Child Kidney Dis.
- 2023 Dec;27(2):70-75.
- doi: 10.3339/ckd.23.019
Dent disease is a rare inherited kidney tubulopathy caused by mutations in either the CLCN5 (Dent disease 1) or OCRL1 (Dent disease 2) genes, and which is often underdiagnosed in... -
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- Tolvaptan: a possible preemptive treatment option in children with autosomal dominant polycystic kidney disease?
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Beak HS, Cho MH
- KMID: 2549737
- Child Kidney Dis.
- 2023 Dec;27(2):76-81.
- doi: 10.3339/ckd.23.021
Tolvaptan is a highly selective vasopressin receptor 2 antagonist that regulates cyclic adenosine monophosphate levels to inhibit both epithelial cell proliferation and chloride ion excretion, two mechanisms known to induce... -
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- Nutcracker syndrome combined with immunoglobulin A nephropathy: two case reports
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Ki SH, Son MH, Park E, Yim HE
- KMID: 2549746
- Child Kidney Dis.
- 2023 Dec;27(2):133-138.
- doi: 10.3339/ckd.23.013
Nutcracker syndrome (NCS) is a disease caused by compression of the left renal vein between the superior mesenteric artery and the abdominal aorta. Immunoglobulin A (IgA) nephropathy (IgAN) is characterized... -
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- A case of cystinuria with a heterozygous SLC3A1 mutation presenting with recurrent multiple renal stones in a 14-year-old boy
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Cho HW, Son MH, Yim HE
- KMID: 2549745
- Child Kidney Dis.
- 2023 Dec;27(2):127-132.
- doi: 10.3339/ckd.23.014
Cystinuria, a genetically inherited disorder, is a rare cause of kidney stones. It is characterized by impaired transport of cystine and amino acids in the proximal renal tubule and the... -
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- Angiotensin receptor blocker induced fetopathy: two case reports and literature review
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Joung J, Cho H
- KMID: 2549744
- Child Kidney Dis.
- 2023 Dec;27(2):121-126.
- doi: 10.3339/ckd.23.022
The administration of angiotensin type 2 receptor blockers (ARBs) during pregnancy is known to cause ARB fetopathy, including renal insufficiency. We aimed to analyze the outcomes of two patients who... -
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- Association of body weight and urinary tract infections during infancy: a nationwide comparative matched cohort study
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Park PG, Kim JH, Ahn YH, Kang HG
- KMID: 2549742
- Child Kidney Dis.
- 2023 Dec;27(2):111-116.
- doi: 10.3339/ckd.23.020
Purpose: This article was to investigate the association between urinary tract infections (UTIs) and high weight status in infancy. Methods: We conducted a nationwide matched cohort study from January 2018 to... -
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- Renal artery stenosis presenting as congenital nephrotic syndrome with hyponatremic hypertensive syndrome in a 2-month-old infant: a case report
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Kim D, Ahn YH, Kang HG, Kim JH, Lim SH
- KMID: 2549743
- Child Kidney Dis.
- 2023 Dec;27(2):117-120.
- doi: 10.3339/ckd.23.017
Here, we present the case of a 2-month-old male infant with hyponatremic hypertensive syndrome resulting from stenosis of the right proximal and mid-renal arteries. The patient exhibited nephrotic-range proteinuria, low... -
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- Nutcracker syndrome in children: review of symptom, diagnosis, and treatment
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Kalantar DS, Park SJ, Shin JI
- KMID: 2549739
- Child Kidney Dis.
- 2023 Dec;27(2):89-96.
- doi: 10.3339/ckd.23.018
Renal nutcracker syndrome (NCS) is the entrapment of the left renal vein between the abdominal aorta and superior mesenteric artery. Although uncommon in pediatric patients, early diagnosis is crucial to... -
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- Efficacy and safety of losartan in childhood immunoglobulin A nephropathy: a prospective multicenter study
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Hyun H, Ahn YH, Park E, Choi HJ, Han KH, Lee JW, Kim SY, Yang EM, Suh JS, Shin JI, Cho MH, Koo JW, Kim KH, Park HW, Ha IS, Cheong HI, Kang HG, Kim SH
- KMID: 2549740
- Child Kidney Dis.
- 2023 Dec;27(2):97-104.
- doi: 10.3339/ckd.23.006
Purpose: Angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers (ARBs) are frequently employed to counteract the detrimental effects of proteinuria on glomerular diseases. However, the effects of ARBs remain poorly... -
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- Hypokalemia as a risk factor for prolonged QT interval and arrhythmia in inherited salt-losing tubulopathy
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Kang SR, Ahn YH, Kang HG, Choi N
- KMID: 2549741
- Child Kidney Dis.
- 2023 Dec;27(2):105-110.
- doi: 10.3339/ckd.23.011
Purpose: To analyze electrocardiograms (ECGs) of patients with a salt-losing tubulopathy (SLT) and to determine the frequency and risk factors for long QT and arrhythmia. Methods: A total of 203 patients... -
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