An infantile case of Hinman syndrome with severe acute renal failure

Vorapong Chaichanamongkol, Masahiro Ikeda, Kenji Ishikura, Yuko Hamasaki, Hiroshi Hataya, Hiroyuki Satoh, Hiroshi Asanuma, Seiichiro Shishido, Masataka Honda

研究成果: Article査読

6 被引用数 (Scopus)

抄録

A 1-year-6-month-old Japanese girl with Hinman syndrome manifested urosepsis and severe obstructive nephropathy. Her voiding cystourethrogram (VCUG) revealed high-grade vesicoureteral reflux with hydronephrosis; urodynamic study was compatible with detrusor-sphincter dyssynergia. She was treated conservatively, including clean intermittent catheterization. At 3 years old, bladder function had not improved, and estimated creatinine clearance was in the subnormal range. Hinman syndrome is a potential cause of acute and chronic renal failure in infancy. Taking account of the possibility of this condition in any neonates or infants who present urinary tract infection (UTI) appears to be necessary, since early recognition and proper management of this syndrome may prevent serious complications.

本文言語English
ページ(範囲)309-311
ページ数3
ジャーナルClinical and experimental nephrology
12
4
DOI
出版ステータスPublished - 2008 8月
外部発表はい

ASJC Scopus subject areas

  • 生理学
  • 腎臓病学
  • 生理学(医学)

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