Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome. (4th August 2020)
- Record Type:
- Journal Article
- Title:
- Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome. (4th August 2020)
- Main Title:
- Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome
- Authors:
- Izumita, Yukie
Nishigaki, Satsuki
Satoh, Mari
Takubo, Noriyuki
Numakura, Chikahiko
Takahashi, Ikuko
Soneda, Shun
Abe, Yoshifusa
Kamasaki, Hotaka
Ohtsu, Yoshiaki
Igaki, Junko
Hasegawa, Yukihiro
Nagasaki, Keisuke - Abstract:
- Abstract: Although Turner syndrome (TS) is frequently associated with congenital anomalies of the kidney‐urinary tract (CAKUT), which is a major cause of pediatric chronic kidney disease, renal function in TS is usually considered normal. The present study aimed to analyze the frequency of renal dysfunction and CAKUT in pediatric patients with TS. Our study included 122 patients with TS between the ages of 2 and 18 years from 30 hospitals across Japan. Clinical data related to renal function and CAKUT were retrospectively collected. The estimated glomerular filtration rate (eGFR) was calculated using the serum creatinine‐based formula recommended by the Japanese Society for Pediatric Nephrology. An eGFR <90 mL/min/1.73 m 2 for two consecutive years was defined as renal dysfunction. Fifteen (13.5%) of 122 patients had CAKUT, and four patients had renal dysfunction (3.2%, 95% confidence interval: 0%‐6.7%). Three of the four did not have CAKUT. Of the CAKUT manifestations, horseshoe kidney, renal hypodysplasia, and multicystic dysplastic kidney were seen in nine, two, and one patient, respectively. Eight of the nine patients with horseshoe kidney had a normal renal function; however, the remaining patient with renal hypodysplasia had renal dysfunction. A small percentage of patients with pediatric TS may had an eGFR below 90 mL/min/1.73 m 2 which was not necessarily associated with CAKUT.
- Is Part Of:
- Congenital anomalies. Volume 60:Number 6(2020)
- Journal:
- Congenital anomalies
- Issue:
- Volume 60:Number 6(2020)
- Issue Display:
- Volume 60, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 60
- Issue:
- 6
- Issue Sort Value:
- 2020-0060-0006-0000
- Page Start:
- 175
- Page End:
- 179
- Publication Date:
- 2020-08-04
- Subjects:
- CAKUT -- horseshoe kidney -- renal function -- turner syndrome
Abnormalities, Human -- Periodicals
616.043 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗ - DOI:
- 10.1111/cga.12384 ↗
- Languages:
- English
- ISSNs:
- 0914-3505
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3410.683000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15013.xml