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792 Possible Causes for Pyramidal Syndrome

  • Pharyngitis

    […] headache, weakness, fatigue, restlessness, sedation, insomnia, mood changes, agitation, personality disorder, impaired speech, tardive dyskinesia, dystonia, tremor, extra-pyramidal[] […] effects, neuroleptic malignant syndrome, coma, postinjection delirium-sedation syndrome CV: orthostatic hypotension, chest pain, tachycardia EENT: amblyopia, rhinitis, pharyngitis[]

  • Polyendocrine - Polyneuropathy Syndrome

    […] hypogonadism, incomplete puberty, progressive non-autoimmune insulin-dependent diabetes mellitus, peripheral demyelinating sensorimotor polyneuropathy, and cerebellar and pyramidal[] syndrome; Subcortical temporal white matter disease, moderate; Cerebellar hypoplasia, mild (in some patients); Hypoplastic pituitary gland (in some patients); [Peripheral[] MalaCards based summary : Polyendocrine-Polyneuropathy Syndrome, is also known as pepns , and has symptoms including ataxia An important gene associated with Polyendocrine-Polyneuropathy[]

  • Pallidopyramidal Syndrome

    Homepage Rare diseases Search Search for a rare disease Parkinsonian-pyramidal syndrome Disease definition Parkinsonian-pyramidal syndrome is a rare, genetic, neurological[] […] parkinsonian-pyramidal syndrome since the first description by Davison in 1954.[] ORPHA:171695 Synonym(s): Pallidopyramidal syndrome Prevalence: - Inheritance: Autosomal recessive Age of onset: Adolescent , Adult ICD-10: G20 OMIM: 168100 168601 260300 UMLS[]

  • Pyramidal Tract Disorder

    Definition A pyramidal syndrome attacks the pyramidal tracts, the neural pathways controlling voluntary movement.[] Drugs that are associated with Pyramidal tract syndrome Pyramidal tract syndrome (168 drugs) Could your condition cause Pyramidal tract syndrome Pyramidal tract syndrome ([] Synonyms (terms occurring on more labels are shown first): pyramidal tract syndrome More information : PubMed search and possibly Wikipedia License: Except as otherwise noted[]

  • Parkinson's Disease Type 9

    syndrome with cognitive/psychiatric features.[] Although the Kufor-Rakeb syndrome has similarities to pallido-pyramidal syndrome, it seems to be distinguished as a separate entity by the presence of dementia and upgaze[] Disease onset varied from 10 to 29 years of age, the latest reported, and the clinical features were highly variable within a wide spectrum of an extrapyramidal-pyramidal[]

  • Behr Syndrome

    In the second decade, they gradually developed gait difficulties due to a moderate spastic pyramidal syndrome and mild cerebellar ataxia.[] Behr syndrome was first described in 1909 as a syndrome of heredofamilial optic atrophy, visual disturbances, nystagmus, and variable pyramidal tract signs.[] A 6-year-old girl with a progressive syndrome of optic atrophy, ataxia, myoclonic epilepsy, urinary incontinence, and pyramidal tract degeneration suggestive of Behr syndrome[]

  • Juvenile Paralysis Agitans of Hunt

    Syndrome [7] occuring in families.[] Syndrome, Parkinsonian-pyramidal syndrome, pallidopyramidal syndrome, Pallidopyramidal Syndrome, PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET, Pallidopyramidal syndrome[] Called also paleostriatal syndrome , pallidal atrophy , pallidal syndrome, and Ramsay Hunt syndrome . Medical dictionary . 2011 .[]

  • T3 Thyrotoxicosis

    The authors concluded that the left pyramidal syndrome was secondary to autoimmune free T3-thyrotoxicosis.[]

  • Autosomal Recessive Spastic Ataxia Type Charlevoix-Saguenay

    The pyramidal syndrome is characterized by rapid tendon reflexes of knee bone and Babinski signs.[] syndrome and peripheral neuropathy Here, we present a 28-year-old male patient with symptoms of gait instability, distal sensory loss and spasticity since 10 years of age[] The pyramidal syndrome is characterised by brisk patellar tendon reflexes and the Babinski sign.[]

  • Neurodegeneration with Brain Iron Accumulation

    Abstract Kufor Rakeb disease (KRD, PARK9) is an autosomal recessive extrapyramidal-pyramidal syndrome with generalized brain atrophy due to ATP13A2 gene mutations.[] (pallido-pyramidal syndrome and hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration).[] Although the Kufor-Rakeb syndrome has similarities to pallido-pyramidal syndrome, it seems to be distinguished as a separate entity by the presence of dementia and upgaze[]

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