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

doi:10.1007/s10157-008-0048-3

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

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	309-311
Number of pages	3
Journal	Clinical and experimental nephrology
Volume	12
Issue number	4
DOIs	https://doi.org/10.1007/s10157-008-0048-3
Publication status	Published - 2008 Aug
Externally published	Yes

Keywords

Acute renal failure
Chronic renal failure
Detrusor-sphincter dyssynergia
Hinman syndrome
Infant
Non-neurogenic neurogenic bladder
Urinary tract infection

ASJC Scopus subject areas

Physiology
Nephrology
Physiology (medical)

Access to Document

10.1007/s10157-008-0048-3

Cite this

@article{57e86bf67ef1459b969126f13f54e2f0,

title = "An infantile case of Hinman syndrome with severe acute renal failure",

abstract = "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.",

keywords = "Acute renal failure, Chronic renal failure, Detrusor-sphincter dyssynergia, Hinman syndrome, Infant, Non-neurogenic neurogenic bladder, Urinary tract infection",

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

year = "2008",

month = aug,

doi = "10.1007/s10157-008-0048-3",

language = "English",

volume = "12",

pages = "309--311",

journal = "Clinical and Experimental Nephrology",

issn = "1342-1751",

publisher = "Springer Japan",

number = "4",

}

TY - JOUR

T1 - An infantile case of Hinman syndrome with severe acute renal failure

AU - Chaichanamongkol, Vorapong

AU - Ikeda, Masahiro

AU - Ishikura, Kenji

AU - Hamasaki, Yuko

AU - Hataya, Hiroshi

AU - Satoh, Hiroyuki

AU - Asanuma, Hiroshi

AU - Shishido, Seiichiro

AU - Honda, Masataka

PY - 2008/8

Y1 - 2008/8

N2 - 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.

AB - 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.

KW - Acute renal failure

KW - Chronic renal failure

KW - Detrusor-sphincter dyssynergia

KW - Hinman syndrome

KW - Infant

KW - Non-neurogenic neurogenic bladder

KW - Urinary tract infection

UR - http://www.scopus.com/inward/record.url?scp=47649103893&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=47649103893&partnerID=8YFLogxK

U2 - 10.1007/s10157-008-0048-3

DO - 10.1007/s10157-008-0048-3

M3 - Article

C2 - 18409063

AN - SCOPUS:47649103893

SN - 1342-1751

VL - 12

SP - 309

EP - 311

JO - Clinical and Experimental Nephrology

JF - Clinical and Experimental Nephrology

IS - 4

ER -

An infantile case of Hinman syndrome with severe acute renal failure

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this