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

  • Hallervorden-Spatz Syndrome

    They may experience involuntary muscle contractions (dystonia) of the head and neck, resulting in repetitive movements and contortions.[ghr.nlm.nih.gov] 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] Neurologically, opisthotonus, rigidity of extremities, dystonia, hyperreflexia, profound emaciation, and bilaterally positive Babinski signs were present.[ncbi.nlm.nih.gov]

  • 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] sign 0003487 Bulbar palsy 0001283 Cognitive impairment Abnormality of cognition Cognitive abnormality Cognitive defects Cognitive deficits Intellectual impairment Mental[rarediseases.info.nih.gov]

  • Autosomal Dominant Sensory Ataxia

    The episodes are triggered by stress, being startled, or sudden movement and are often associated with muscle twitching.[disabled-world.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] Babinski sign MedGen UID: 19708 • Concept ID: C0034935 • Finding A reflex characterized by upward movement of the great toe and an outward movement of the rest of the toes[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 4

    Those with SCA will also often experience numbness, tingling or pain in their limbs, uncontrolled muscle tensing, muscle wasting and muscle twitching.[medicalmarijuanainc.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] sign 0003487 Cerebellar atrophy Degeneration of cerebellum 0001272 Distal sensory impairment Decreased sensation in extremities 0002936 Hyporeflexia Decreased reflex response[rarediseases.info.nih.gov]

  • Spinocerebellar Ataxia Type 23

    […] 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] […] 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] It is characterized by gait ataxia, dysarthria , slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.[rarediseases.info.nih.gov]

  • Spastic Ataxia with Congenital Miosis

    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] sign 33 HP:0003487 11 dysdiadochokinesis 33 HP:0002075 12 abnormal conjugate eye movement 33 HP:0000549 Symptoms via clinical synopsis from OMIM: 58 Neurologic Central Nervous[malacards.org]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    […] 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] Common clinical features of FRDA Ataxia (truncal and limb types) Absent or reduced tendon reflexes Extensor plantar reflexes (Babinski's sign) Peripheral neuropathy Atrophy[forgottendiseases.org]

  • Spinocerebellar Ataxia Type 5

    Those with SCA will also often experience numbness, tingling or pain in their limbs, uncontrolled muscle tensing, muscle wasting and muscle twitching.[indycann.org] The onset of symptoms is usually in the third or fourth decade of life; however, more subtle clinical manifestations can start in early childhood.[ncbi.nlm.nih.gov] Hyperreflexia and a positive Babinski sign are commonly presently. Mild cognitive impairment and depression have been seen in a minority of patients.[disorders.eyes.arizona.edu]

  • 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] Over half of the cases display pyramidal symptoms, hyperreflexia, and positive Babinski sign with little to no spasticity.[elsevier.es]

  • Autosomal Dominant Spastic 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.medscape.com] Hyperreflexia and a positive Babinski sign are commonly presently. Mild cognitive impairment and depression have been seen in a minority of patients.[disorders.eyes.arizona.edu]

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