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342 Possible Causes for Broad-Based Gait, Hypoplasia of Dentate Nucleus, Multiperforated Patent Foramen Ovale

  • Friedreich Ataxia

    The unsteadiness further progresses to a broad-based,… Read More mitochondrial disorders In metabolic disease: Mitochondrial disorders …iron homeostasis is present in Friedreich[britannica.com] 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] With progression, gait becomes broad-based, with frequent losses of balance requiring intermittent and then constant support.[doi.org]

    Missing: Multiperforated Patent Foramen Ovale
  • Adams-Oliver Syndrome Type 5

    From Wikidata Jump to navigation Jump to search syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs Adams Oliver syndrome Limb, scalp and skull defects Aos Congenital scalp defects with distal limb anomalies Limb scalp and skull defects[…][wikidata.org]

    Missing: Broad-Based Gait
  • Duchenne Muscular Dystrophy

    The longer survival of patients with Duchenne muscular dystrophy due to advances in clinical care has increased the incidence of Duchenne muscular dystrophy-associated cardiomyopathy, a nearly consistent feature in the third decade of life. A 26-year-old patient with Duchenne muscular dystrophy experienced[…][ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Subacute Combined Degeneration of Spinal Cord

    His gait was broad based with spinal ataxia. Decreased graphaesthesia was found on the lower limbs, the lower part of the trunk and on the upper limbs.[neuroanatomy.wisc.edu]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Diabetic Pseudotabes

    In addition to the broad-based, stamping gait, which becomes worse when patients try to walk in the dark, abnormal findings included diminished vision owing to optic atrophy[std-aid.com] Ataxia of gait is evident, and results of heel-to-sin and finger-to-nose testing are abnormal.[std-aid.com]

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

    A 29-year-old man developed acute cerebellar ataxia following Epstein-Barr virus infection. Serum IgG and IgM antibodies reacted with both nuclear and cytoplasmic elements of neurons. Western blot revealed IgG binding to the 34- and 29-kd bands and IgM binding to the 44-, 37-, and 29-kd bands. The IgM reactivity[…][ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Tabes Dorsalis

    The patient's ataxia was evident as she walked with a broad-based gait.[lksom.temple.edu]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Hereditary Areflexic Dystasia

    From Wikidata Jump to navigation Jump to search human disease Hereditary areflexic dystasia, Roussy-LC)vy type Hereditary areflexic dystasia, Roussy-Lévy type ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA Roussy-Levy Syndrome Roussy-Lévy syndrome edit English Roussy–Lévy syndrome human disease Hereditary[…][wikidata.org]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Ataxic Cerebral Palsy

    Patients with ataxic cerebral palsy will usually have a broad-based gait, i.e. they walk with their feet unusually far apart.[medhelp.org] Showing of 9 Percent of people who have these symptoms is not available through HPO Autosomal recessive inheritance 0000007 Broad-based gait Wide based walk 0002136 Cerebellar[rarediseases.info.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale
  • Ataxia Telangiectasia

    Ataxia-telangiectasia (A-T) is a multisystem disease caused by a genetic defect located on the long arm of chromosome 11 (11p22-23). The gene defect results in the loss of A-T-mutated protein, subsequently leading to unrepaired DNA fractures and defects in the signal transduction pathway. As a result,[…][ncbi.nlm.nih.gov]

    Missing: Hypoplasia of Dentate Nucleus Multiperforated Patent Foramen Ovale

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