athetosis/seizures

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Ukurasa 1 kutoka 38 matokeo

Benign epileptic seizures in infancy followed by paroxysmal choreo-athetosis during adolescence.

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Ingia / Ingia

Cough, vomiting; convulsions. [athetosis].

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Ingia / Ingia

[Double athetosis with Bielschowsky bodies--their histological features and distribution in the lateral pallidum].

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Ingia / Ingia

This report analyzes a rare case of double athetosis with Bielschowsky bodies. These bodies are pleomorphic intra-neuronal PAS positive deposits mainly found in the lateral palladium of both sides. Clinically the patient was diagnosed as "double athetosis" and mild mental retardation. In her

Athetosis in typhoid fever.

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Ingia / Ingia

A case of typhoid fever with neuropsychiatric features is described. These comprised confusion and delirium, meningism, a single major convulsion and bilateral athetoic movements. Athetosis has not previously been described in typhoid fever and must now be added to the long list of neuropsychiatric

Cerebellar stimulation for cerebral palsy spasticity, function, and seizures.

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Ingia / Ingia

Chronic cerebellar stimulation (CCS) applied to the superio-medial cortex reduces generalized cerebral spasticity, athetoid movements, and seizures. Eighteen clinics have reported on 600 cerebral palsy (CP) patients who comprise 90% of those treated with CCS. CP patients have varying degrees of

Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencing.

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Ingia / Ingia

Whole exome sequencing combined with homozygosity mapping comprises a genetic diagnostic tool to identify genetic defects in families with multiple affected members, compatible with presumed autosomal recessively inherited neurometabolic/neurogenetic disease. These tools were applied to a family

Congenital granuloprival hypoplasia of cerebellar and hippocampal cortex.

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Ingia / Ingia

Two siblings with congenital granule cell hypoplasia of the cerebellum and hippocampus are reported. The patients, both male, showed severe psychomotor retardation, microcephaly, hypotonia, athetosis, and seizures; they died at the ages of 3 7/12 years and 5 10/12 years, respectively. Postmortem

Bilateral striatal lesions in childhood.

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Ingia / Ingia

From 1983 to 1991, 13 patients were identified with a clinical radiologic association characterized by acute or persistent neurologic dysfunction and bilateral lesions in the basal ganglia region demonstrated by ultrasound, computed tomography, or magnetic resonance imaging. Initial clinical

Motor severity in children with cerebral palsy studied in a high-resource and low-resource country.

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Ingia / Ingia

OBJECTIVE To compare the patterns of motor type and gross motor functional severity in preschool-aged children with cerebral palsy (CP) in Bangladesh and Australia. METHODS We used comparison of 2 prospective studies. A total of 300 children with CP were aged 18 to 36 months, 219 Australian children

Genetic factors in athetoid cerebral palsy.

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Ingia / Ingia

Within the cerebral palsy syndromes, athetosis is most commonly causally associated with serious perinatal complications. Genetic factors are thought to play a lesser role, although the risk of recurrence in siblings has been suggested to be as high as 10%. We have conducted a clinical study of 22

[Paroxysmal dyskinesias - disorder categories, their causes and treatment].

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Ingia / Ingia

Paroxysmal dyskinesias refer to category of abnormal involuntary movements, such as chorea, dystonia, athetosis, ballism or their various configurations. Depending on the type of seizure, sudden movement, stress, emotions, coffee or alcohol may be the trigger factors. Acute seizures are

Clinical and neuropathological findings in severe athetoid cerebral palsy: a comparative study of globo-Luysian and thalamo-putaminal groups.

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Ingia / Ingia

We divided cases of severe athetoid cerebral palsy originating perinatally into two groups neuropathologically, the "globo-Luysian group" (GL) and the "thalamo-putaminal group" (TP). The major abnormal sites in GL were the pallidum and subthalamic nucleus, and in TP the thalamus and putamen. The

[De Barsy-Moens-Dierckx syndrome: unusual course in a neonate].

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Ingia / Ingia

We report about a premature infant with a De Barsy-Moens-Dierckx-syndrome, which is a rare cutaneo-oculo-cerebral malformation-syndrome. It is defined by the combination of a progeroid aspect, cutis laxa, growth retardation, cornea clouding, mental retardation and athetoid movements. Furthermore,

[Paroxysmal dyskinesias].

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala

Ingia / Ingia

BACKGROUND Paroxysmal dyskinesias are uncommon movements disorders that consist on recurrent brief episodes characterized by attacks with any combination of dystonia, chorea, athetosis or ballismus. CONCLUSIONS The pathophysiology of paroxysmal dyskinesias is unclear at the present time. An

Magnesium metabolism in Huntington's chorea.

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Ingia / Ingia

Human magnesium deficiency states are known to be associated with tremor, choreiform and athetoid movements, delirium and convulsions. In order to assess a recent report of altered magnesium metabolism in Huntington's chorea, 6 patients with the disease have been studied with complete balance

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