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apraxias/kopfschmerz
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Gait apraxia and headache.
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[Ruptured distal anterior cerebral artery aneurysm and diagnostic dyspraxia: a case report].
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A case of ruptured distal anterior cerebral artery aneurysm presenting with diagnostic dyspraxia is presented. A 54-year-old female was referred to our hospital with the complaint of sudden onset of headache followed by disturbance of consciousness. CT and MRI revealed subarachnoid hemorrhage with
[A 81-year-old man with dementia, gait disturbance, hemiparesis, and sympathetic apraxia].
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We present a 81-year old male who developed dementia, gait disturbance and right hemiparesis. He was well until the age of 74 when he developed a hemorrhagic infarction in the right occipital region, which left him left homonymous hemianopsia. One year later he had one TIA attack consisting of
[Diagnostic image (284). A man with Horner's syndrome, ipsilateral headache and dysphasia].
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A 56-year-old man presented with sudden dysphasia and dyspraxia. He had noticed a small left pupil and had suffered from left-sided headache two weeks previously. MRI revealed dissection of the left inner carotid artery.
[A case of astrocytoma of corpus callosum presented diagnostic dyspraxia].
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A case of astrocytoma whose first clinical presentation was diagnostic dyspraxia was reported. A 38-year-old right-handed male experienced funny motion of his left hand triggered by voluntary movement of his right hand. One day, he tried to insert a coin into the vending machine with his right hand,
Reversible splenial lesion syndrome after blood transfusion presents callosal disconnection syndrome: A case report.
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BACKGROUND
Reversible splenial lesion syndrome (RESLES) is a reversible condition with an excellent prognosis in most patients. The clinical features include altered states of consciousness, delirium, headache, and seizures, but no callosal disconnection syndromes have been described in
[A Mexican case of massive nonencephalitic neurocysticercosis].
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Neurocysticercosis is common in Asia, Africa and South America including Mexico. A diagnosis of neurocysticercosis was made neuroradiologically in an 8-year-old Mexican girl, who had suffered from learning difficulties for a year, and subsequently developed headache, vomiting, gait disturbance,
Supratentorial hydatid cyst with cerebellar signs: a rare case of diaschisis.
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BACKGROUND
Intracranial hydatid disease has a distinct predominance in the pediatric age group and still causes serious problems in endemic areas.
METHODS
A 7-year-old girl admitted with a 3-month history of illness involving the main symptoms of ataxic gait, apraxia, headache, and tremor and with
Endoscopic third ventriculostomy for treatment of noncommunicating syringomyelia associated with a Chiari I malformation and hydrocephalus: case report and pathophysiological considerations.
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OBJECTIVE
A Chiari I malformation associated with syringomyelia and hydrocephalus is a rare condition. We report the successful use of endoscopic third ventriculostomy for the treatment of this pathological entity. The successful use of this technique in such a case has not been previously
[Multiple sclerosis with higher cerebral dysfunction: a case report].
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Higher cerebral dysfunctions such as aphasia, apraxia and agnosia have seldom been reported in multiple sclerosis (MS). 12 year-old right-handed boy felt unsteadiness of the body and headache for several days. Two months later, he had the same episode and complained of visual disturbance, and
The syndrome of hydrocephalus in young and middle-aged adults (SHYMA).
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OBJECTIVE
Currently, headache, nausea/vomiting, visual changes, and altered mental status are accepted as indications for the evaluation of hydrocephalus in children; while dementia, gait apraxia, and urinary incontinence remain indications in the elderly. The clinical presentation of hydrocephalus
[Persistent neurological sequelae due to cerebral malaria in a cohort of children from Mali].
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BACKGROUND
Several neurological complications are associated with cerebral malaria (CM). However, few long-term data from childhood survivors have been published.
METHODS
A cross-sectional study was carried out in Mali among children followed from 1999 to 2002 after serious and complicated malaria.
[Large distal anterior cerebral artery aneurysm associated with azygos anterior cerebral artery: case report].
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A 51-year-old woman presented with a distal anterior cerebral artery aneurysm (DACAA) manifesting as severe headache and monoparesis of the left lower limb. Computed tomography revealed subarachnoid hemorrhage in the interhemispheric fissure, bilateral sylvian fissures, and basal cistern, and a
Central nervous system involvement in severe arterial hypertension of childhood.
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The case histories of 125 children with hypertension and no apparent primary CNS disease were analyzed for neurological symptoms or complications. Eleven children had neurological symptoms of high blood pressure. In only one of these patients was the diagnosis of arterial hypertension made before
Frontal agraphia, (including a case report).
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Frontal agraphia has always been a subject of interest, although very few documented case reports have been published. A 57 year old male clerk, suffering from adenocarcinoma of the signoid colon, presented with mild headache and difficulty in writing. Minor features of dysphasia could be detected,
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