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1,551 Possible Causes for Episodic Ataxia

  • Spinocerebellar Ataxia Type 6

    The three allelic disorders, episodic ataxia type 2, familial hemiplegic migraine, and SCA6, have overlapping clinical features.[ncbi.nlm.nih.gov] Ataxia type 2.[ncbi.nlm.nih.gov] Spinocerebellar ataxia type 6 (SCA6), episodic ataxia type 2 (EA2) and familial hemiplegic migraine (FHM) have been known as allelic disorders, which are caused by the alteration[ncbi.nlm.nih.gov]

  • Ataxia

    Episodic ataxias (EAs) are rare channelopathies characterized by recurrent ataxia and vertigo, having eight subtypes.[ncbi.nlm.nih.gov] PRRT2 gene mutations cause paroxysmal kinesigenic dyskinesia (PKD), infantile convulsions, hemiplegic migraine, and episodic ataxia.[ncbi.nlm.nih.gov] Episodic ataxia: With episodic ataxia, people have recurring troubles with movement and balance.[my.clevelandclinic.org]

  • Episodic Ataxia

    GeneReviews/NCBI/NIH/UW entry on Episodic Ataxia Type 1, Episodic Ataxia with Myokymia, Hereditary Cerebellar Ataxia with Neuromyotonia GeneReviews/NCBI/NIH/UW entry on Episodic[en.wikipedia.org] ataxia edit English episodic ataxia hereditary ataxia characterized by sporadic bouts of ataxia with or without continuous muscle movement Isaacs syndrome episodic ataxia[wikidata.org] Clinical spectrum of episodic ataxia type 2.[ncbi.nlm.nih.gov]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Most ADCAs are spinocerebellar ataxias (SCA) or episodic ataxias.[blueprintgenetics.com] Episodic Ataxia Type I. In: NORD Guide to Rare Disorders; Lippincott Williams & Wilkins. Philadelphia, PA 2003:600-01. Burns RS. Episodic Ataxia Type II.[rarediseases.org] ataxia type 1 Episodic ataxia type 3 Episodic ataxia type 4 Episodic ataxia type 5 Episodic ataxia type 6 Episodic Ataxia Unknown type Epstein syndrome Exposure to Medications[sanfordresearch.org]

  • Paroxysmal Exertion-Induced Dyskinesia

    PED can be associated with paroxysmal dystonic choreathetosis with episodic ataxia and spasticity, benign familial infantile seizures (BFIE), infantile convulsions and choreoathetosis[orpha.net] PED can be associated with paroxysmal dystonic choreathetosis with episodic ataxia and spasticity , benign familial infantile seizures (BFIE), infantile convulsions and choreoathetosis[rarediseases.info.nih.gov]

  • Infantile Convulsions and Choreoathetosis

    The association with other paroxysmal disorders such as migraine, with or without aura, hemiplegic migraine, episodic ataxia and tics has also been described.[orpha.net] Examples include: mutations of the KCNA1 potassium channel subunit gene in epilepsy with episodic ataxia type 1 39 ; rare mutations within the ATP1A2 sodium/potassium pump[doi.org] A peculiar form of autosomal dominant PKD with episodic ataxia and spasticity has been mapped at chromosome 1p. 67 Another PKD locus (PKC1) has been mapped at the ICCA locus[doi.org]

  • Autosomal Dominant Spastic Ataxia Type 1

    EA Episodic ataxia with myokymia Eam ataxia, episodic, with myokymia AEM Aemk paroxysmal ataxia with neuromyotonia, hereditary myokymia with periodic ataxia Episodic ataxia[diseaseinfosearch.org] Most ADCAs are spinocerebellar ataxias (SCA) or episodic ataxias.[blueprintgenetics.com] Patients may have migrainous episodes as well as ataxia, and some patients with the SCA6 mutation may present with episodic ataxia.[movementdisorders.org]

  • Autosomal Recessive Spinocerebellar Ataxia 18

    Most ADCAs are spinocerebellar ataxias (SCA) or episodic ataxias.[blueprintgenetics.com] Autosomal dominant ataxias include the spinocerebellar ataxias and episodic ataxias.[bcm.edu] Episodic Ataxia Type I. In: NORD Guide to Rare Disorders; Lippincott Williams & Wilkins. Philadelphia, PA 2003:600-01. Burns RS. Episodic Ataxia Type II.[rarediseases.org]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    Most ADCAs are spinocerebellar ataxias (SCA) or episodic ataxias.[blueprintgenetics.com] , mental retardation, and dysequilibrium syndrome AR 3 4 CACNA1A Migraine, familial hemiplegic, Episodic ataxia, Spinocerebellar ataxia 6, Epileptic encephalopathy, early[blueprintgenetics.com] Otol Neurotol 22:506-511, 2001 FAMILIAL EPISODIC CEREBELLAR ATAXIA There are two common variants of episodic ataxia syndrome, called EA1 and EA2, as well as a number of other[tchain.com]

  • Hereditary Cerebellar Degeneration

    Most ADCAs are spinocerebellar ataxias (SCA) or episodic ataxias.[blueprintgenetics.com] […] and episodic ataxias.[medlink.com] Autosomal dominant ataxias include the spinocerebellar ataxias and episodic ataxias.[bcm.edu]

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