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31 Possible Causes for Muscle Twitch, Onset of Dysarthria in Third Decade of Life, Seizure

  • Hallervorden-Spatz Syndrome

    Clinical features Dystonia Dysarthria Spasticity Choreoathetosis Parkinsonism Hyperreflexia Extensor toe signs Onset in first to third decade of life Gait change / loss of[ncbi.nlm.nih.gov] The patient presented with a slowly progressive illness with seizures, extrapyramidal symptoms, cerebellar ataxia, dementia, spasticity, myoclonic movements and a severe demyelinating[ncbi.nlm.nih.gov] They may experience involuntary muscle contractions (dystonia) of the head and neck, resulting in repetitive movements and contortions.[ghr.nlm.nih.gov]

  • Episodic 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.com] Mutations in CACNA1A encoding a neuronal calcium channel and ATP1A2 encoding an ion pump cause episodic ataxia, hemiplegic migraine, and seizures.[ncbi.nlm.nih.gov] This abnormality can cause muscle cramping, stiffness, and continuous, fine muscle twitching that appears as rippling under the skin.[ghr.nlm.nih.gov]

  • Neurodegeneration with Brain Iron Accumulation

    muscle twitches) Muscle weakness Stiffness of limbs Dystonia: Involuntary muscle contractions that cause repetitive movements or distorted postures Dysphagia (difficulty in[dovemed.com] Clinical features Dystonia Dysarthria Spasticity Choreoathetosis Parkinsonism Hyperreflexia Extensor toe signs Onset in first to third decade of life Gait change / loss of[ncbi.nlm.nih.gov] […] abnormalities and cognitive decline… BPAN BPAN (Beta-propeller Protein-associated Neurodegeneration) is an NBIA disorder that is characterized by childhood developmental delay and seizures[nbiacure.org]

  • 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] Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolemia and borderline hypoalbuminemia.[mendelian.co] The episodes are triggered by stress, being startled, or sudden movement and are often associated with muscle twitching.[disabled-world.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] This results in a high frequency of randomly distributed mtDNA mutations and thus a wide range of phenotypes, including seizures, neuropathy, and cerebellar ataxia [1, 2].[ncbi.nlm.nih.gov] The episodes are triggered by stress, being startled or sudden movement, and often are associated with muscle twitching.[mayoclinic.org]

  • 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] CONVULSIONS, TYPE 3A Nav1.2 (K69/3) FEBRILE SEIZURES ASSOCIATED WITH AFEBRILE SEIZURES BENIGN FAMILIAL INFANTILE CONVULSIONS, TYPE 3 Nav1.6 (K87A/10) CEREBELLAR ATROPHY,[neuromab.ucdavis.edu] […] 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]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    […] 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] 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]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    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] […] tonic-clonic seizures).[neuroweb.us]

  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar 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] About 30% of patients develops other seizure types, such as hemiconvulsions, motor seizures or generalized tonic-clonic seizures 42.[centogene.com] […] of muscles or parts of muscles, without any rhythm or pattern, occurring in various brain disorders) 19q SCA16 ( ITPR1 ) 39 yrs (20–66) 1–40 years Head and hand tremor 8q[en.wikipedia.org]

  • Spinocerebellar Ataxia Type 13

    […] jerks or twitches (myoclonic jerks). [1] [2] [3] [4] Other symptoms may include speech difficulty ( dysarthria ), difficulty eating ( dysphagia ), slowness of movements ([rarediseases.info.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] The p.Arg423His variant has also been associated with mild cognitive impairment and seizures.[ncbi.nlm.nih.gov]

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