dyskinesias/febră

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Fever producing ballismus in patients with choreoathetosis.

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We report two children with choreoathetoid cerebral palsy who had intermittent, severe, paroxysmal episodes of ballismus in response to febrile illnesses. These episodes lasted for hours and were difficult to control, requiring large doses of haloperidol or phenytoin. Differentiation from seizures

Severe hyperthermia during tetrabenazine therapy for tardive dyskinesia.

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We recently observed a 45-year-old patient with a history of psychiatric illness who presented with severe hyperthermia (rectal temperature above 41 degrees C) with intense rhabdomyolysis and liver cytolysis during tetrabenazine therapy for neuroleptic tardive dyskinesia. In addition to

Tardive dyskinesia due to Rocky Mountain spotted fever: case report.

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Fever-induced protracted ballismus in choreoathetoid cerebral palsy.

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Pain and fever arising from the common bile duct and not associated with jaundice; report of 2 cases of choledocholithiasis treated by choledochostomy and 1 of post-cholecystectomy biliary dyskinesia relieved by vagotomy.

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[A case of involuntary movements probably produced by low doses of phenytoin intoxication].

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A 49-year-old woman, who presented gait disturbance, orofacial dyskinesia, choreoathetosis and slightly cloudy consciousness, was admitted to our hospital on February 7, 1986. She had a slight fever and sore throat for the previous ten days. She had been treated for hypothyroidism as well as

[Involuntary movements observed in a patient with Russian spring summer encephalitis].

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A 38-year-old woman had an episode of headache, fever and convulsion in October, 1993. She became alert in two weeks, though weakness and atrophy remained in the upper limb muscles. She was diagnosed as Russian spring summer encephalitis (RSSE) based on several serological studies. Three kinds of

Clinical findings and prevalence of the mutation associated with primary ciliary dyskinesia in Old English Sheepdogs.

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BACKGROUND Primary ciliary dyskinesia (PCD) is generally a recessively inherited disorder characterized by dysfunction of motile cilia. A mutation in a new causative gene (CCDC39) has been identified in the Old English Sheepdog (OES). OBJECTIVE To describe the clinical findings and the molecular

PANDAS: the search for environmental triggers of pediatric neuropsychiatric disorders. Lessons from rheumatic fever.

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Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection (PANDAS) is a relatively new diagnostic construct applied to children or adolescents who develop, and have repeated exacerbations of, tic disorders and/or obsessive-compulsive disorder following group A

Chorea in fifty consecutive patients with rheumatic fever.

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Rheumatic fever (RF) remains a significant public health problem in developing countries. Although its incidence has been declining in developed areas, several outbreaks of RF have been identified in the United States since 1985. To study the prevalence and clinical features of Sydenham's chorea

A possible mechanism of primary ciliary dyskinesia: a case of a segmental defect in ciliary microtubules.

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We report here a 13-year-old woman with cough, sputum and fever. The patient had both chronic sinusitis and bronchitis. Chest X-ray and computed tomographic scan of the chest revealed mucous bronchial filling and bronchiectasia in bronchi of bilateral lower lobes, right middle lobe and left upper

Refractory status epilepticus complicated by drug-induced involuntary movements.

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New onset refractory status epilepticus (NORSE) is a neurological emergency and difficult to treat condition. We report a case of involuntary movements resulting from thiopentone sodium infusion during the management of refractory status epilepticus. A young woman was admitted with fever and NORSE

Behavior outbursts, orofacial dyskinesias, and CSF pleocytosis in a healthy child.

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Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis represents a new category of immune-mediated neurologic disorders. Viral encephalitis is often the presumptive diagnosis because of the acute neurologic changes, cerebrospinal fluid lymphocytic pleocytosis, and occasional hyperthermia. We report

Acute Rheumatic Fever: An Evidence-Based Approach To Diagnosis And Initial Management.

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Acute rheumatic fever is an inflammatory reaction involving the joints, heart, and nervous system that occurs after a group A streptococcal infection. It typically presents as a febrile illness with clinical manifestations that could include arthritis, carditis, skin lesions, or abnormal movements.

Hypermetabolic Syndrome and Dyskinesia After Neurologic Surgery for Labrune Syndrome: A Case Report.

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A 20-year-old man with a rare neurodegenerative disease developed hypermetabolic symptoms with dyskinesia after a third ventriculostomy for hydrocephalus. The initial presentation was concerning for an acute dystonic reaction after metoclopramide was administered for nausea. He concurrently

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