Evidence that congenital hydrocephalus is a precursor to idiopathic normal pressure hydrocephalus in only a subset of patients

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Idiopathic Normal Pressure Hydrocephalus

Idiopathic normal pressure hydrocephalus (iNPH) is a potentially reversible neurodegenerative disease commonly characterized by a triad of dementia, gait, and urinary disturbance. Advancements in diagnosis and treatment have aided in properly identifying and improving symptoms in patients. However, a large proportion of iNPH patients remain either undiagnosed or misdiagnosed. Using PubMed searc...

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Is normal pressure hydrocephalus becoming less idiopathic?

Normal pressure hydrocephalus (NPH) has posed a challenge to neurologists for 5 decades. Difficulties in understanding its pathophysiology have hindered efforts to diagnose it and to develop a better approach to selecting patients for shunt surgery. We know that many patients with NPH have CSF absorption difficulty as measured by resistance to CSF outflow (Rout). The problem is that many with n...

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Treatment of Idiopathic Normal Pressure Hydrocephalus by Persian Medicine: A Case Report

Idiopathic normal pressure hydrocephalus (iNPH) is a chronic disease in adults. The standard treatment in this type of hydrocephalus is shunting which is accompanied by some complications and there is also uncertainty about response to treatment. Therefore, surgery is performed in only 10-20% of the cases with iNPH. Currently, oral acetazolamide and repetitive lumbar puncture for drainage of th...

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Idiopathic normal pressure hydrocephalus-- a report of 73 patients.

In 1973 we reported results of ventricular shunting in 28 patients with idiopathic normal pressure hydrocephalus. The present report consists of a three year follow-up of the latter (series 1), and an additional 45 patients (series 2) are presented for further insight into the conclusions drawn from the original experiences.

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Normal Pressure Hydrocephalus Presentation with a Large Pseudomeningocele

Background and Importance: This interesting case is about the presence of normal pressure hydrocephalus and a large pseudomeningocele at the same time after 13 months of posterior fossa surgery. Although the occurrence of a pseudomeningocele following posterior fossa surgery is not so rare, such a late large pseudomeningocele development with signs and symptoms of NPH after 13 months of surgery...

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ژورنال

عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry

سال: 2006

ISSN: 0022-3050

DOI: 10.1136/jnnp.2006.108761