Literature DB >> 21996110

Twelve-year experience with Hinman-Allen syndrome at a single center.

Mesrur Selcuk Silay1, Orhan Tanriverdi, Tuna Karatag, Gul Ozcelik, Kaya Horasanli, Cengiz Miroglu.   

Abstract

OBJECTIVE: To report the long-term follow-up results of patients with Hinman-Allen syndrome (HAS) at our institution.
METHODS: The data from 22 children with HAS were retrospectively analyzed. The patients were followed up every 3-6 months with serial physical examinations, voiding charts, urine culture, postvoid residual urine volume determination, serum creatinine measurement, and urinary imaging. The follow-up time was calculated from the day of the first visit to the day of the latest dimercaptosuccinic acid scan. Urotherapy, pharmacotherapy, clean intermittent catheterization, biofeedback therapy, and surgery were performed sequentially and/or combined, depending on the disease course. Renal deterioration was defined as any presence of a new scar or cortical thinning compared with the findings from the first dimercaptosuccinic acid scan. Upper urinary tract deterioration was defined as the persistence or progression of hydronephrosis on ultrasonography.
RESULTS: The mean age at referral was 9.18 ± 3.36 years (range 2-14), and the mean follow-up period was 80.90 ± 19.57 months (range 54-144). Conservative therapy resulted in improvement of the bladder function in 14 patients; however, 8 patients required surgery owing to failure of this approach. Asymptomatic bacteriuria developed in one half of the children (n = 11, 50%), and in 6 (22.7%), ≥1 febrile urinary tract infection developed. None of the patients had upper urinary tract deterioration; however, renal deterioration developed in 3 patients (13.6%). The mean creatinine levels had remained stable at the end of the follow-up.
CONCLUSION: Close follow-up at a single institution and proactive treatment resulted in successful stabilization of HAS in most of our children with HAS.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21996110     DOI: 10.1016/j.urology.2011.08.018

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  6 in total

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Journal:  J Am Soc Nephrol       Date:  2014-08-21       Impact factor: 10.121

Review 2.  Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation.

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Journal:  Pediatr Nephrol       Date:  2013-07-09       Impact factor: 3.714

3.  LRIG2 mutations cause urofacial syndrome.

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Journal:  Am J Hum Genet       Date:  2013-01-11       Impact factor: 11.025

4.  Diagnosis and management of bladder bowel dysfunction in children with urinary tract infections: a position statement from the International Children's Continence Society.

Authors:  Stephen Yang; Michael E Chua; Stuart Bauer; Anne Wright; Per Brandström; Piet Hoebeke; Søren Rittig; Mario De Gennaro; Elizabeth Jackson; Eliane Fonseca; Anka Nieuwhof-Leppink; Paul Austin
Journal:  Pediatr Nephrol       Date:  2017-10-03       Impact factor: 3.714

5.  End-stage renal disease in a Down syndrome patient caused by delayed diagnosis of nonneurogenic bladder: A case report.

Authors:  Ga Eun Kim; Dal Sik Sin; Seung Soo Kim; Chang-Ho Lee; Nam-Jun Cho; Eun Young Lee
Journal:  Medicine (Baltimore)       Date:  2019-04       Impact factor: 1.817

6.  Evaluation of functional lower urinary tract dysfunction in children: are the physicians complying with the current guidelines?

Authors:  Mesrur Selcuk Silay; Ahmet Ruknettin Aslan; Erim Erdem; Zafer Tandogdu; Serdar Tekgul
Journal:  ScientificWorldJournal       Date:  2013-04-23
  6 in total

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