Create issue ticket

226 Possible Causes for Cerebellar Disease, Muscle Hypotonia, Truncal Ataxia

  • Dandy-Walker Syndrome

    Dandy-Walker syndrome congenital disorder of nervous system Upload media Wikipedia Instance of disease, developmental defect during embryogenesis Subclass of cerebellar disease[commons.wikimedia.org] […] cerebellar vermis and fourth ventricle.[ 3 ] Infants with DWM may present with early signs such as vomiting, sleepiness, irritability, convulsions, unsteadiness and lack of muscle[ncbi.nlm.nih.gov] […] to Diseases , 10.1007/978-3-319-59749-2_19 , (389-406) , (2017) .[ncbi.nlm.nih.gov]

  • Dysequilibrium Syndrome

    ataxia was used to identify the mutation.[ncbi.nlm.nih.gov] Stefano D'Arrigo, Lucia Viganò, Maria Grazia Bruzzone, Michela Marzaroli, Ioannis Nikas, Daria Riva and Chiara Pantaleoni , Diagnostic Approach to Cerebellar Disease in Children[doi.org] Clinical features include cerebellar ataxia, early-onset cataracts, mild to severe cognitive impairment, hypotonia, and muscle weakness.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 1

    Neurological examination 5 years after onset revealed slow eye movement with nystagmus as well as limb and truncal ataxia.[ncbi.nlm.nih.gov] Duration of disease was similar in the Huntington’s disease and degenerative cerebellar diseases groups.[doi.org] […] twitch 0002380 Gait imbalance Abnormality of balance Abnormality of equilibrium Imbalanced walk [ more ] 0002141 Generalized hypotonia Decreased muscle tone Low muscle tone[rarediseases.info.nih.gov]

  • Acute Cerebellar Ataxia

    PATIENT AND METHOD: This patient developed symptoms of ACA, including nausea, vertigo, severe limb and truncal ataxia, and bilateral spontaneous continuous horizontal nystagmus[ncbi.nlm.nih.gov] Four previously published reports of cerebellar ataxia with Lyme disease are reviewed.[pediatricneurologybriefs.com] This neurologic syndrome was characterized by sudden onset of muscle hypotonia and inability to sit or walk, with no other specific neurologic or systemic symptoms.[ncbi.nlm.nih.gov]

  • Alcoholic Cerebellar Degeneration

    ataxia Unsteady gait Nystagmus May be clinically asymptomatic in some individuals Laboratory No specific laboratory abnormalities Radiology description Atrophy of the anterior[pathologyoutlines.com] Stance – a broad-based gait is noted in cerebellar disease 2.[geekymedics.com] Decreased muscle tone Nystagmus Involuntary, rapid oscillation of the eyeballs in a horizontal, vertical, or rotary direction, with the fast component maximal toward the[merckmanuals.com]

  • Autosomal Recessive Spinocerebellar Ataxia 18

    , truncal .[malacards.org] To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] ataxia.[synapse.koreamed.org]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    […] the extremities, truncal ataxia, increased reflexes in the lower extremities, and intellectual disability.[malacards.org] […] tumor, paraneoplastic syndrome, Creutzfeldt-Jakob disease, Whipple’s disease, celiac disease, autoimmune thyroiditis, and anti-GAD associated cerebellar ataxia have been[blogs.nejm.org] Limb and truncal ataxia and seizures may be present.[movementdisorders.org]

  • Cerebellar Mass Lesion

    — gait abnormalities Truncal Ataxia versus Appendicular Ataxia Truncal Ataxia Caused by lesions confined to the cerebellar vermis Affect primarily the medial motor systems[brainaacn.org] Clinical Signs of Disease in the Cerebellar Hemispheres A lesion in one cerebellar hemisphere will cause motor deficits on the ipsilateral side of the body.[casemed.case.edu] (hypotonia), 8) slurred speech (ataxic dysarthria), and 9) abnormal eye movements (nystagmus [4] Loss of Expressions: Cerebellum is also involved in some cognitive functions[howmed.net]

  • Autosomal Recessive Spinocerebellar Ataxia

    SCAR16 is characterized by truncal and limb ataxia resulting in gait instability.[uniprot.org] To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] Ataxia, both truncal and cerebellar, is present. Mobility is impaired from early childhood and eventually requires assistance.[disorders.eyes.arizona.edu]

  • Leigh's Disease

    The second attack was noted one month later, to be associated with hypotonia and truncal ataxia.[ncbi.nlm.nih.gov] diseases classified elsewhere G32.81 Cerebellar ataxia in diseases classified elsewhere G32.89 Other specified degenerative disorders of nervous system in diseases classified[icd10data.com] Abstract An 11-month-old boy with muscle hypotonia and neurologic deteriorations had lactic acidosis, pyruvic acidemia and alaninemia due to deficiency of the pyruvate dehydrogenase[ncbi.nlm.nih.gov]

Similar symptoms