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16 Possible Causes for Lateral Medullary Syndrome, Muscle Twitch, Onset of Dysarthria in Third Decade of Life

  • Spinocerebellar Ataxia Type 1

    (atrophy); and muscle twitches (fasciculations).[ghr.nlm.nih.gov] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.com] Over time, SCA1 may cause mental impairment, numbness, tingling, or pain in the arms and legs and uncontrolled muscle tensing, wasting, and twitches.[rarediseases.info.nih.gov]

  • Autosomal Dominant Sensory Ataxia

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] Medulla (CN 8, 9, 10, 12) Lateral medullary syndrome/Wallenberg PICA Medial medullary syndrome/Dejerine ASA Pons (CN 5, 6, 7, 8) Upper dorsal pontine syndrome/Raymond Céstan[en.wikipedia.org] The episodes are triggered by stress, being startled, or sudden movement and are often associated with muscle twitching.[disabled-world.com]

  • Episodic Ataxia

    […] associated with infarction 5 in the posterior inferior cerebellar artery territory (lateral medullary or Wallenberg syndrome) include ipsilateral hemiataxia, vertigo, dysarthria[ajnr.org] This abnormality can cause muscle cramping, stiffness, and continuous, fine muscle twitching that appears as rippling under the skin.[ghr.nlm.nih.gov] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.com]

  • Spastic Ataxia with Congenital Miosis

    Infarction of the posterior inferior cerebellar artery causes lateral medullary syndrome (Wallenberg's syndrome) with hemiataxia, vertigo, dysarthria, ptosis and miosis Space-occupying[patient.info] Muscle findings of only fasiculations and the workup of such* Definition Muscle twitching is caused by minor muscle contractions in the area, or uncontrollable twitching of[flashcardmachine.com] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com]

  • Ataxia

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] associated with infarction 5 in the posterior inferior cerebellar artery territory (lateral medullary or Wallenberg syndrome) include ipsilateral hemiataxia, vertigo, dysarthria[ajnr.org] The episodes are triggered by stress, being startled or sudden movement, and often are associated with muscle twitching.[mayoclinic.org]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    […] cystic kidney disease type 1 autosomal dominant Job syndrome, see autosomal dominant hyper-IgE syndrome Autosomal dominant lateral temporal lobe epilepsy, see autosomal dominant[mygenomics.com] The episodes are triggered by stress, being startled or sudden movement, and often are associated with muscle twitching.[mayoclinic.org] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com]

  • Autosomal Dominant Spastic Ataxia Type 1

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] cystic kidney disease type 1 autosomal dominant Job syndrome, see autosomal dominant hyper-IgE syndrome Autosomal dominant lateral temporal lobe epilepsy, see autosomal dominant[mygenomics.com] (atrophy); and muscle twitches (fasciculations).[ghr.nlm.nih.gov]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    medullary, Weber's, Lacunar stroke ) Sleep disorders Insomnia · Hypersomnia · Sleep apnea ( Obstructive, Ondine's curse ) · Narcolepsy · Cataplexy · Kleine-Levin · Circadian[thefullwiki.org] […] of muscles or parts of muscles, without any rhythm or pattern, occurring in various brain disorders) 19q SCA16 39 yrs (20-66) 1-40 years Head and hand tremor 8q SCA17 ( TBP[psychology.wikia.com] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] cystic kidney disease type 1 autosomal dominant Job syndrome, see autosomal dominant hyper-IgE syndrome Autosomal dominant lateral temporal lobe epilepsy, see autosomal dominant[mygenomics.com] […] of muscles or parts of muscles, without any rhythm or pattern, occurring in various brain disorders) 19q SCA16 39 yrs (20-66) 1-40 years Head and hand tremor 8q SCA17 ( TBP[psychology.wikia.com]

  • Spinocerebellar Ataxia Type 20

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] Medullary (Wallenberg syndrome) o PICA o Vestibular nuclei: vertigo, N/V, nystagmus (away from lesion) o Inferior cerebellar peduncle: ipsilateral limb ataxia o Nucleus ambiguous[neurosurgerystudent.blogspot.com] Tremor, sensory loss, twitches of facial muscles, and slowness and stiffness similar to that seen in Parkinson’s disease have been observed in SCA-14.[ataxiacenter.umn.edu]

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