Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1438
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dc.contributor.authorSiddangouda B Patil, Kshitiz Ranka Vinay S Kundargi Ashok N Biradar Nikhil A Patil.-
dc.date.accessioned2019-11-27T07:23:09Z-
dc.date.available2019-11-27T07:23:09Z-
dc.date.issued2015-
dc.identifier.issn23496940-
dc.identifier.urihttp://hdl.handle.net/123456789/1438-
dc.description.abstractHinman syndrome or non-neurogenic neurogenic bladder is a rare clinical condition which is characterized by non-neurogenic urinary bladder dysfunction. It is a diagnosis of exclusion and patient presents with characteristics of a neurogenic bladder with external sphincter dyssynergia but without evidence of any neurologic alteration. The underlying pathology is not known. Bladder training and medical treatment have been recognized as effective management. However, when there is established damage to the upper urinary system or chronic renal failure, surgery is preferred over conservative treatment. Due to the low incidence of the disease, there is still no consensus for the most adequate treatment or management. We report the case of a pediatric patient presented with recurrent retention of urine with dysfunctional voiding and compromised renal functions. As patient already presented with upper urinary tract damage hence underwent successful surgical treatment for the same.en_US
dc.language.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectChronic renal failure, Hinman syndrome, Non-neurogenic neurogenic bladderen_US
dc.titleHinman Syndrome - Diagnosis and Management: A Rare Case Reporten_US
dc.typeArticleen_US
Appears in Collections:Faculty of Urology

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