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19 Possible Causes for Cerebellar Ataxia during Episodes

  • Ondine Syndrome

    Soon thereafter, an apneic episode occurred during a sleep and advanced to ataxic respiration, and the patient died.[ncbi.nlm.nih.gov] ataxia in the left upper and lower limbs.[ncbi.nlm.nih.gov] […] dysarthria, nystagmus, left central facial paralysis, paralysis of the left soft palate, dysphagia, decreased superficial sensation over the right face and upper limb, and cerebellar[ncbi.nlm.nih.gov]

  • Familial Hemiplegic Migraine Type 2

    Abstract Familial hemiplegic migraine (FHM), a rare autosomal dominant subtype of migraine with aura, has been linked to two chromosomal loci, 19p13 and 1q23. Mutations in the Na K -ATPase alpha2 subunit gene, ATP1A2, on 1q23 have recently been shown to cause familial hemiplegic migraine type 2 (FHM2). We sequenced the[…][ncbi.nlm.nih.gov]

  • Acute Cerebellar Ataxia

    Sixteen months after the recurrence of ataxia, CT and MRI revealed marked cerebellar atrophy.[ncbi.nlm.nih.gov] No further augmentation of ataxia or of cerebellar atrophy was observed during following 30 months.[ncbi.nlm.nih.gov] Thirty-three months later, cerebellar symptoms recurred without apparent preceding episode, and persisted.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 6

    ataxia is a dominantly inherited paroxysmal cerebellar neurological disorder characterized by episodes of cerebellar ataxia, often accompanied by nausea, vertigo, and headache[doi.org] Episodic ataxia type 1 (EA1) presents interictal myokymia during and between episodes due to mutations in a potassium voltage-gated channel gene, located on chromosome 12.[doi.org] […] all those with cerebellar signs. 2 - 6 Some FHM families without cerebellar signs have been assigned to chromosome 1q, whereas others are not linked to any known loci. 7 Episodic[doi.org]

  • Episodic Ataxia

    AUTOSOMAL dominant episodic ataxias are a clinically and genetically heterogeneous group of conditions characterized by recurrent paroxysmal attacks of cerebellar ataxia starting[doi.org] Episodic ataxia type 2 is an autosomal dominant disorder characterized by the recurrence of acetazolamide-responsive spells of cerebellar ataxia, usually starting during childhood[ncbi.nlm.nih.gov] Background Episodic ataxia type 2 is an autosomal dominant disorder characterized by the recurrence of acetazolamide-responsive spells of cerebellar ataxia, usually starting[doi.org]

  • Cerebellar Ataxia

    ataxia and altered consciousness during febrile illnesses.[ncbi.nlm.nih.gov] Topka, Reversible cerebellar gait ataxia with postural tremor during episodes of high pyrexia, Clinical Neurology and Neurosurgery, 98, 3, (227), (1996). David J.[oadoi.org] Here, we report on a 34-year-old female presenting with a new ATP1A3-related entity involving a relapsing encephalopathy characterized by recurrent episodes of cerebellar[ncbi.nlm.nih.gov]

  • Generalized Myotonia of Thomsen

    Cerebellar Ataxia usually starting during childhood or adolescence.[puneataxiasupport.wordpress.com] EPISODIC ATAXIA Autosomal dominant Episodic Ataxias are a clinically and genetically heterogeneous group of conditions characterized by recurrent paroxysmal attacks of generalized[puneataxiasupport.wordpress.com] Two forms of Episodic Ataxia have been identified: Episodic Ataxia 1 and Episodic Ataxia 2.[puneataxiasupport.wordpress.com]

  • Presenile Dementia with Bone Cysts

    It is characterized by chronic progressive neurological deterioration with cerebellar ataxia, milder spasticity and mental decline.[thefreelibrary.com] During these episodes, loss of motor faculties and hypotonia are observed, with coma and death in some cases.[thefreelibrary.com] The evolution is characterized by episodes of major and rapid deteriorations following different triggers, such as minor head trauma, febrile infections and acute fright.[thefreelibrary.com]

  • Superficial Siderosis of the Central Nervous System

    Two patients developed cerebellar ataxia, three of them present transient focal neurological episodes, one dementia and, the last one, the diffuse superficial siderosis of[ncbi.nlm.nih.gov] No clinical progression was observed during follow-up (2-11 years) in three of them. The patient with cerebral amyloid angiopathy progresses to dementia.[ncbi.nlm.nih.gov]

  • Hartnup Disease

    However, some people with Hartnup disease have episodes during which they exhibit other signs, which can include skin rashes; difficulty coordinating movements ( cerebellar[ghr.nlm.nih.gov] ataxia ); and psychiatric symptoms, such as depression or psychosis.[ghr.nlm.nih.gov] These episodes are typically temporary and are often triggered by illness, stress, nutrient-poor diet, or fever.[ghr.nlm.nih.gov]

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