Create issue ticket

3,081 Possible Causes for Cerebellar Ataxia, Hypoplasia of Dentate Nucleus, Multiperforated Patent Foramen Ovale

  • Adams-Oliver Syndrome Type 5

    34 Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Limb-girdle muscular dystrophy Muscular dystrophy Witkop syndrome Brugada syndrome[checkrare.com] Phocomelia ectrodactyly deafness sinus arrhythmia Cerebellar hypoplasia tapetoretinal degeneration Charcot-Marie-Tooth disease Autosomal dominant spondyloepiphyseal dysplasia[checkrare.com] ataxia, deafness, and narcolepsy Achondrogenesis type 2 Tangier disease Charcot-Marie-Tooth disease type 2F Niemann-Pick disease type B Macrocephaly mesodermal hamartoma[checkrare.com]

  • Friedreich Ataxia

    Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.[doi.org] The neuropathology was also similar and included hypoplasia of spinal cord and dorsal root ganglia, loss of large axons in dorsal roots, and atrophy of the dentate nucleus[ncbi.nlm.nih.gov] ataxia with retained reflexes.[ncbi.nlm.nih.gov]

    Missing: Multiperforated Patent Foramen Ovale
  • Chronic Alcoholism

    There was a progressive development of parkinsonism, cerebellar ataxia, and mental deterioration by the time he was 32.[ncbi.nlm.nih.gov] Others develop for non-hereditary reasons, such as alcoholic cerebellar ataxia. What Is Cerebellar Ataxia? Cerebellar ataxia is a symptom, not a distinct disorder.[promises.com] * Affects nearly every organ system: NEURO – Affects both peripheral nervous system (peripheral neuropathy) and central nervous sytem : Cognitive dysfunction, Cerebellar degeneration[errolozdalga.com]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Infectious Mononucleosis

    Infectious mononucleosis (IM) complicated with a neurological manifestation, including acute cerebellar ataxia, Guillain-Barre syndrome, meningitis, encephalitis, cranial[ncbi.nlm.nih.gov] Ataxia Guillain-Barre syndrome Pancreatitis Myocarditis Pneumonia Lung disease Lymphocytosis Weakened immune system To find out more about these other possible illnesses,[americanpregnancy.org] ataxia. 4 The role of plasmapheresis in treating Guillain—Barré variants is not clear.[nejm.org]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Autosomal Dominant Mental Retardation Type 21

    SPECTRIN-ASSOCIATED AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA Is also known as infantile-onset spinocerebellar ataxia-psychomotor delay syndrome cerebellar ataxia, autosomal recessive[mendelian.co] The causative gene in SCA21, TMEM240, is highly expressed in the cerebellum, dentate gyrus, putamen and caudate nucleus.[pediatricneurologybriefs.com] ; dementia (mild); 23% of all AD cerebellar ataxia; genetic testing available SCA4 (autosomal dominant type 4) 16q22.1-ter; pleckstrin homology domain-containing protein,[accesspharmacy.mhmedical.com]

    Missing: Multiperforated Patent Foramen Ovale
  • Helsmoortel-van der Aa Syndrome

    ataxia type II Autosomal dominant cerebellar ataxia type III Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome[se-atlas.de] The causative gene in SCA21, TMEM240, is highly expressed in the cerebellum, dentate gyrus, putamen and caudate nucleus.[pediatricneurologybriefs.com] SPECTRIN-ASSOCIATED AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA Is also known as infantile-onset spinocerebellar ataxia-psychomotor delay syndrome cerebellar ataxia, autosomal recessive[mendelian.co]

    Missing: Multiperforated Patent Foramen Ovale
  • Hypothyroidism

    Rarely it can present with neurologic problems like reversible cerebellar ataxia, dementia, peripheral neuropathy, psychosis and coma.[ncbi.nlm.nih.gov] Cerebellar ataxia. Psychosis. Encephalopathy. Patients can go on to develop myxoedema coma (see below).[patient.info] Hypothyroidism should be considered in all cases of cerebellar ataxia as it is a reversible cause of ataxia. [Indexed for MEDLINE] Free full text[ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Strabismus

    […] autosomal dominant cerebellar ataxia type 1, characterized by the adult-onset of unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria,[orpha.net] These patients presented with a form of cerebellar ataxia with slow saccadic eye movements4.[scielo.br] Keywords: Spinocerebellar ataxia, ataxic dysarthria, perceptual analysis, acoustic analysis, cerebellar degenerative disorders, cognitive impairment, language impairment,[openarchive.ki.se]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Bronchogenic Carcinoma

    Neurological examination revealed left cerebellar ataxia. Neuroimaging showed multiple cerebellar metastases with cerebellar hemorrhage adjacent to the tentorium.[ncbi.nlm.nih.gov] A 58-year-old male presented with a rare case of brain metastatic bronchogenic carcinoma with human chorionic gonadotropin (hCG) production causing cerebellar hemorrhage with[ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Cerebellar Hemorrhage

    Thirty-two months later, he was readmitted with complaints of occipital, neck, and shoulder pain as well as cerebellar ataxia.[ncbi.nlm.nih.gov] Neurological examination revealed left cerebellar ataxia. Neuroimaging showed multiple cerebellar metastases with cerebellar hemorrhage adjacent to the tentorium.[ncbi.nlm.nih.gov] Subsequent magnetic resonance imaging demonstrated cerebellar hemorrhage and progression in the downward herniation of the tonsils.[ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale

Similar symptoms