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253 Possible Causes for Babinski Sign, Hypotension, Spasticity - Hyperreflexia

  • Aromatic L-Amino Acid Decarboxylase Deficiency

    […] clinical features suggesting spasticity.[jn.nutrition.org] […] aromatic L-amino acid decarboxylase deficiency who developed serious cardiac rhythm disturbances during treatment with intravenous dopamine and norepinephrine for severe hypotension[ncbi.nlm.nih.gov] When the neurotransmitters are not being produced correctly, there are problems with the nervous system. 0000271 Autosomal recessive inheritance 0000007 Babinski sign 0003487[rarediseases.info.nih.gov]

  • Autosomal Dominant Spastic Paraplegia Type 10

    ) is a rare type of hereditary spastic paraplegia that can present as either a pure form of spastic paraplegia with lower limb spasticity, hyperreflexia and extensor plantar[orpha.net] […] hour sleep–wake disorder Jet lag CSF Intracranial hypertension Hydrocephalus / NPH Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension[maria-online.com] sign 0003487 Distal sensory impairment Decreased sensation in extremities 0002936 Hyperreflexia in upper limbs 0007350 Impaired distal vibration sensation 0006886 Leg muscle[rarediseases.info.nih.gov]

  • Autosomal Dominant Spastic Paraplegia Type 17

    Central Nervous System: spasticity hyperreflexia clonus difficulty standing walking on tiptoes more Clinical features from OMIM: 607584 UMLS symptoms related to Spastic Paraplegia[malacards.org] […] hour sleep–wake disorder Jet lag CSF Intracranial hypertension Hydrocephalus / NPH Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension[maria-online.com] Affiliated tissues include globus pallidus, skin and bone, and related phenotypes are babinski sign and lower limb hyperreflexia Disease Ontology : 12 A hereditary spastic[malacards.org]

  • Autosomal Dominant Spastic Paraplegia Type 8

    24, Autosomal Recessive Symptoms via clinical synopsis from OMIM: 57 Neurologic Central Nervous System: spasticity hyperreflexia clonus difficulty standing walking on tiptoes[malacards.org] Autonomic features are impotence and postural hypotension (most marked at times of fluid removal by dialysis).[neuroweb.us] Other common symptoms of HSP are urinary urgency and frequency, hyperactive reflexes, difficulty with balance, clonus, Babinski’s sign, diminished vibration sense in the feet[sp-foundationorg.presencehost.net]

  • Autosomal Dominant Spastic Paraplegia Type 6

    […] usually presents in late adolescence or early adulthood as a pure phenotype of lower limb spasticity with hyperreflexia and extensor plantar responses, as well as mild bladder[orpha.net] […] hour sleep–wake disorder Jet lag CSF Intracranial hypertension Hydrocephalus / NPH Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension[maria-online.com] Related phenotypes are babinski sign and talipes equinovarus Disease Ontology : 12 A hereditary spastic paraplegia that has material basis in mutation in the ZFYVE27 gene[malacards.org]

  • Autosomal Dominant Spastic Paraplegia Type 31

    24, Autosomal Recessive Symptoms via clinical synopsis from OMIM: 57 Neurologic Central Nervous System: spasticity hyperreflexia clonus difficulty standing walking on tiptoes[malacards.org] Autonomic features are impotence and postural hypotension (most marked at times of fluid removal by dialysis).[neuroweb.us] Babinski sign was negative. Video gait analysis was performed, which showed internal rotation of the hips and feet while walking and running.[omicsonline.org]

  • Autosomal Recessive Spastic Paraplegia Type 56

    , hyperreflexia, lower-limb weakness and decreased vibration sensation 37 yrs, 22 – 60 yrs AD Uncomplicated KIAA0196 (SPG8) DNA Sequencing 25 – 42 yrs AR Uncomplicated/ Paraplegin[1pdf.net] Progressive & Disabling in 2nd & 3rd decade in some patients Cerebellar Spastic-Ataxic gait EOM: Gaze-evoked horizontal nystagmus; Upbeat nystagmus; Ocular dysmetria Orthostatic hypotension[neuromuscular.wustl.edu] Affiliated tissues include globus pallidus , and related phenotypes are lower limb hyperreflexia and babinski sign Disease Ontology : 12 A hereditary spastic paraplegia that[malacards.org]

  • Autosomal Dominant Spastic Paraplegia Type 4

    Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia[ncbi.nlm.nih.gov] A POPULATION-BASED APPROACH Proceedings Vai 2007 An unexpected association between intracranial hypotension and split cord malformation Proceedings Vai 2006 Linkage analysis[unipa.it] Neurological examination disclosed mild spasticity and weakness in the legs, hyperreflexia in all limbs, and bilateral Babinski sign.[bmcmedgenet.biomedcentral.com]

  • Autosomal Recessive Spastic Paraplegia Type 7

    , hyperreflexia, lower-limb weakness and decreased vibration sensation 37 yrs, 22 – 60 yrs AD Uncomplicated KIAA0196 (SPG8) DNA Sequencing 25 – 42 yrs AR Uncomplicated/ Paraplegin[1pdf.net] He experienced pollakiuria but neither constipation nor orthostatic hypotension.[nature.com] People with this form of spastic paraplegia may also have hyperreflexia in the arms, dysarthria, dysphagia, nystagmus, mild hearing loss, scoliosis, foot arch elevation, sensory[ivami.com]

  • Pallidopyramidal Syndrome

    […] and hyperreflexia, and hemiplegic gait.[neurologyindia.com] Parkinsonism w orthostatic hypotension Parkinsonism with orthostatic hypotension Parkinsons variant Pigmentary pallidal degeneration Progressive supranuclear ophthalmoplegia[icd9data.com] 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[rarediseases.info.nih.gov]

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