Create issue ticket

21 Possible Causes for Abnormal Gait, Cerebellar Disease, Cold-Induced Muscle Cramps

  • Acute Cerebellar Ataxia

    Four previously published reports of cerebellar ataxia with Lyme disease are reviewed.[pediatricneurologybriefs.com] walking Speech disturbances with slurred speech and changes in tone, pitch, and volume Visual complaints Abnormal eye movements Headache Nausea and vomiting Lightheadedness[cookchildrens.org] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Alcoholic Cerebellar Degeneration

    Stance – a broad-based gait is noted in cerebellar disease 2.[geekymedics.com] Cerebellar ataxia differs from gait problems due to abnormalities in other parts of the nervous system, such as the abnormal gait seen in Parkinson’s disease, normal pressure[hopkinsmedicine.org] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Subacute Cerebellar Degeneration

    walking.[rarediseases.info.nih.gov] cerebellar degeneration in Hodgkin's disease.[malacards.org] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Early-Onset Cerebellar Ataxia

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] The main presenting symptom was abnormal gait (100%). Ataxia of gait and limbs and normal or increased tendon reflexes were found in all cases.[doi.org] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Cerebellar Ataxia with Peripheral Neuropathy Type 2

    Autosomal recessive, X-linked, autosomal dominant Cerebellar ataxias are a highly heterogeneous group of genetic disorders distinguished by abnormal wide-based gait, irregular[centogene.com] […] for balance control in cerebellar disease 2008 National College of Occupational Therapists Conference, Newcastle Vestibular processing for balance control in cerebellar disease[www6.plymouth.ac.uk] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Autosomal recessive, X-linked, autosomal dominant Cerebellar ataxias are a highly heterogeneous group of genetic disorders distinguished by abnormal wide-based gait, irregular[centogene.com] To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Hoyeraal-Hreidarsson Syndrome

    Abnormality of eye movement Unsteady gait Squamous cell carcinoma of the skin Abnormality of the fingernails Bone marrow hypocellularity Abnormality of the liver Dermal atrophy[mendelian.co] From Wikidata Jump to navigation Jump to search a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive[wikidata.org] This rare disease shares clinical features with dyskeratosis congenita and, together, they are recognized as a group of disorders caused by telomere dysfunction.[ncbi.nlm.nih.gov]

  • Cognitive Impairment with or without Cerebellar Ataxia

    Autosomal recessive, X-linked, autosomal dominant Cerebellar ataxias are a highly heterogeneous group of genetic disorders distinguished by abnormal wide-based gait, irregular[centogene.com] To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome in specified disease NEC G32.81 ICD-10[icd10data.com] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

  • Myoadenylate Deaminase Deficiency

    MRI may reveal severe cerebellar atrophy.[neuroweb.us] Walking and Ataxia 415 Case 66 A Man with Progressive Neuropathy and Congestive Heart Failure 422 Case 67 An Elderly Woman with a Progressive Neuropathy 429 Case 68 A Young[books.google.com] .8344A G, n-DNA mutations (POLG1, POLG2, SLC25A4, CI0orf2, RRM2B, TK2 and OPA1) MNGIE: TYMF Mitochondrial DNA depletion syndrome Clinical manifestations of mitochondrial disease[sites.google.com]

  • Autosomal Dominant Myoglobinuria

    Refsum disease Refsum disease (RD) is a peroxisomal disorder clinically characterized by pigmentary retinopathy, cerebellar ataxia, mixed motor-sensory neuropathy and elevated[scielo.br] The first child presented with abnormal gait with difficulty to initiate movement. The second child had stiffness and gait abnormality precipitated by cold weather.[hkjpaed.org] […] dysfunction with exercise intolerance, cramps and acute painful rhabdomyolysis or myoglobinuria (with or without myalgia) induced by fever, fasting or prolonged exercise,[neuroweb.us]

Similar symptoms