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1,094 Possible Causes for Babinski Sign, Hyperactive Brainstem Reflexes, Pseudobulbar Palsy Dysarthria

  • Juvenile Primary Lateral Sclerosis

    - Hypereflexia - Hypertonia / spasticity / rigidity / stiffness - Motor deficit / trouble - Muscle weakness / flaccidity - Pseudobulbar signs / spasmodic laugh and cry -[] […] tendon reflexes, and Babinski signs.[] Hyperreflexia is another key feature of PLS as seen in patients presenting with the Babinski's sign.[]

  • Adult Primary Lateral Sclerosis

    Accompanying emotional lability (inappropriate laughing or crying) - as with pseudobulbar palsies.[] […] tendon reflexes, and Babinski signs.[] Affiliated tissues include brain, testes and cortex, and related phenotypes are dysphagia and babinski sign OMIM : 58 Although primary lateral sclerosis (PLS) is similar to[]

  • Amyotrophic Lateral Sclerosis Type 2

    Amyotrophic lateral sclerosis (ALS) is a progressive and generally fatal neurodegenerative disorder. Most cases are sporadic, but high familial incidence is observed occasionally. Amyotrophic lateral sclerosis 2 (ALS2) is one of many subtypes of familial ALS. It has been related to mutations in the ALS2 gene, a[…][]

    Missing: Hyperactive Brainstem Reflexes
  • Amyotrophic Lateral Sclerosis Type 4

    Accompanying emotional lability (inappropriate laughing or crying) - as with pseudobulbar palsies.[] […] tendon reflexes, and Babinski signs.[] During neurological examination, pyramidal signs can be observed. ALS4 patients show hyperreflexia, have brisk deep-tendon reflexes and the Babinski sign is present.[]

  • Upper Motor Neuron Disease

    Accompanying emotional lability (inappropriate laughing or crying) - as with pseudobulbar palsies.[] […] tendon reflexes, and Babinski signs.[] Babinski sign One of the most often signs of the upper motor neuron syndrome is the Babinski sign.[]

  • Pallidopyramidal Syndrome

    Postural Instability & EP Features :  Falls—backward  Poor postural reflexes  Rigidity –axial  Dysarthria—spastic,  Hypophonic  ataxic  Frontal release signs  Pseudobulbar[] Showing of 32 100% of people have these symptoms Parkinsonism 0001300 30%-79% of people have these symptoms Abnormal autonomic nervous system physiology 0012332 Babinski sign[] INHERITED CREUTZFELDT-JAKOB DISEASE Is also known as inherited cjd Related symptoms: Seizures Nystagmus Muscle weakness Tremor Babinski sign SOURCES: ORPHANET SCTID More info[]

    Missing: Hyperactive Brainstem Reflexes
  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    […] tendon reflexes, and Babinski signs.[] sign 0003487 Dysphagia Poor swallowing Swallowing difficulties Swallowing difficulty [ more ] 0002015 Infantile onset Onset in first year of life Onset in infancy [ more[] In about 25% of cases, ALS begins with brainstem symptoms (dysarthria, difficulty swallowing) followed by extremity weakness.[]

    Missing: Pseudobulbar Palsy Dysarthria
  • Pseudobulbar Palsy

    A 28-year-old, previously healthy, normotensive woman suddenly developed an acute pseudobulbar palsy with dysarthria, dysphagia, hypernasal voice and mild right arm paresis[] brainstem reflexes (eg, jaw jerk), the dissociation of automatic and volitional movements of the bulbar muscles with preservation of automatic movements, and the absence[] All patients showed medically intractable seizures, complex partial seizures with secondary generalization and clinical symptoms of pseudobulbar palsy, including dysarthria[]

    Missing: Babinski Sign
  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    palsy (labileaffect, spasticspeech, dysarthria,brisk jawjerk, and gag reflex)LMN Weakness Muscle atrophy Fasciculations Cramps Attenuated or absentreflexes Bulbar palsy[] […] tendon reflexes, and Babinski signs.[] sign 62% Male, female distribution ratio 1:1 Biochemical study: Low plasma citrate and elevated pyruvate levels and resulting low citrate/pyruvate ratio have been observed[]

  • Autosomal Recessive Spastic Paraplegia Type 20

    Troyer syndrome is characterized by progressive spastic paraparesis, dysarthria, pseudobulbar palsy, distal amyotrophy, short stature, and subtle skeletal abnormalities.[] sign 0003487 Cognitive impairment Abnormality of cognition Cognitive abnormality Cognitive defects Cognitive deficits Intellectual impairment Mental impairment [3] This gene[] There was hyperreflexia in both upper and lower limbs and spastic paraplegia with a bilateral Babinski sign.[]

    Missing: Hyperactive Brainstem Reflexes