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735 Possible Causes for Dyskinesia, Generalized Dystonia, Myopathy

  • Meige Syndrome

    Deep brain stimulation of the globus pallidus internus (GPi DBS) is effective in the treatment of primary segmental and generalized dystonia.[] 2015 ICD-9-CM Diagnosis Code 333.82 Orofacial dyskinesia 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 333.82 is a billable medical code that can[] Deep brain stimulation for primary generalized dystonia: long-term outcomes. Arch Neurol 2009;66:465–470. 6. Jankovic J.[]

  • Adult-Onset Cervical Dystonia Type DYT23

    DYT1 dystonia typically presents as early onset, generalized dystonia, starting in the legs.[] DYT-PRRT2 Paroxysmal kinesigenic dyskinesia AD DYT10 DYT-MR-1 Paroxysmal non-kinesigenic dyskinesia AD DYT8 DYT-SLC2A1 Paroxysmal exertion-induced dyskinesia AD DYT18 a Due[] COL6A1 Bethlem myopathy COL6A2 Bethlem myopathy type 1 COL6A3 Bethlem myopathy type 2 COL12A1 Borjeson-Forssman-Lehmann syndrome PHF6 Brody myopathy ATP2A1 Brunner syndrome[]

  • Writer's Cramp

    Two cases are reported in which simple writer's cramp turned into dystonic writer's cramp without progression to generalized dystonia.[] […] report two monochorionic twins that progressively developed, between ages 5 and 10, a combination of episodic neurological disorders including paroxysmal exercise-induced dyskinesia[] SIGNIFICANCE: Our findings may suggest pathophysiological differences between focal and generalized dystonia, and may also point to an inferior sensitivity of SEPs in detecting[]

  • Primary Torsion Dystonia

    Fifteen of them presented with the typical DYT1 phenotype (early, limb-onset generalized dystonia without spread to craniocervical muscles), four had limb-onset dystonia with[] Moreover, a previous 11C-diprenorphine PET study investigating levodopa-induced dyskinesias found reduced opioid receptor availability in PD with but not without dyskinesias[] Adult-onset acid maltase deficiency is an inherited lysosomal skeletal-muscle disease characterized by progressive myopathy and respiratory failure, for which there is no[]

  • McLeod Neuroacanthocytosis Syndrome

    Clincial features include chorea, oromandibular dystonia (which may be mutilating) or generalized dystonia, phonic tics, feeding/ tongue protrusion dystonia, head drops, ‘[] Weight loss due to feeding dyskinesia: A presenting symptom of neuroacanthocytosis.[] McLeod myopathy revisited – more neurogenic and less benign.[]

  • Oromandibular Dystonia

    Cases of inherited cranial dystonia have been reported, often in conjunction with DYT1 generalized dystonia.[] Male gender, orobuccolingual dyskinesias (facial grimacing, lip biting, tongue dyskinesias, platysma contractions and bruxism) and better response to botulinum toxin injections[] Colchicine,Cyclosporine の併用により myopathy を呈した Behcet 病の 1 症例. 臨床神経 2000; 40(3): 301 2. 池田昭夫, 松本理器, 大原信司, 國枝武治, 柴崎 浩, 白樫義知, 梶 龍兒.[]

  • Spasmodic Torticollis

    This form of focal dystonia is unlikely to spread beyond the neck and shoulders or become generalized dystonia.[] Although expensive, btx treatment is recommended for involuntary neck movements of tardive dystonia but not yet for the classic buccolingual dyskinesia.[] ., GABA) such as described in parkinsonian syndrome (dopamine) or the interruption of a specific pathway that causes and improves a dyskinesia is desirable.[]

  • Idiopathic Camptocormia

    […] was a case of generalized dystonia with camptocormia.[] Similar findings have only been reported recently in a few cases of camptocormia secondary to Parkinson disease or tardive dyskinesia.[] The cause of camptocormia in idiopathic PD is a focal myopathy.[]

  • Familial Dyskinesia and Facial Myokymia

    dystonia 4) Generalized Movements of one or both of the legs, trunk and some other part of the body Unilateral facial muscle contractions patient will have bouts of this[] Familial dyskinesia with facial myokymia (FDFM) is an autosomal dominant disorder that is exacerbated by anxiety.[] View full list of genes Congenital Myopathy and Distal Myopathy NGS panel Published 22/01/2018 Congenital Myopathy and[]

  • Movement Disorder

    Dystonia may affect the entire body (generalized dystonia) or one part of the body (focal dystonia). Functional movement disorder.[] We describe a 13-year-old girl who had features of both paroxysmal kinesigenic dyskinesia and paroxysmal nonkinesigenic dyskinesia that was misdiagnosed as refractory epilepsy[] […] syndrome (MSS) is a recessively inherited multisystem disorder caused by mutations in SIL1 and characterized by cerebellar atrophy with ataxia, cataracts, a skeletal muscle myopathy[]

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