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361 Possible Causes for Ataxia, Behavior Problem, Spasticity - Hyperreflexia

  • Hyponatremia

    They are primarily central nervous system (CNS) manifestations, such as irritability, restlessness, lethargy, muscular twitching, spasticity and hyperreflexia, all of which[aafp.org] Moderate - personality change, muscle cramps and weakness, confusion, ataxia. Severe - drowsiness.[patient.info] behavior. [21] Psychosis after a seizure is relatively common, occurring in between 6 and 10% of people. [22] Often people do not remember what occurred during this time.[en.wikipedia.org]

  • Primary Progressive Multiple Sclerosis

    Affected individuals may have tremors, muscle stiffness (spasticity), exaggerated reflexes (hyperreflexia), weakness or partial paralysis of the muscles of the limbs, difficulty[icdlist.com] Spastic paraparesis and progressive ataxia are principal symptoms in this subset of patients.[symptoma.com] Abstract HDLS (Hereditary Diffuse Leukodystrophy with Spheroids) is a hereditary leukodystrophy whose main clinical manifestations include parkinsonism, spasticity, and ataxia[ncbi.nlm.nih.gov]

  • Subacute Combined Degeneration of Spinal Cord

    Neurological findings include numbness, loss of vibratoty and joint position sense, sense of proprioception, hyperreflexia, spasticity, weakness and extensor plantar responses[ispub.com] […] syndrome dorsal, tumor Nothnagel's syndrome Claude's syndrome Other Alternating hemiplegia Cerebellum lateral ( Dysmetria Dysdiadochokinesia Intention tremor ) medial ( Cerebellar[ipfs.io] He had hyperreflexia, bilateral Babinski signs and absent ankle jerks. Tone was spastic.[neurology.org]

  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

    This feature can vary from lower limb hyperreflexia with positive Babinski sign, with or without gait abnormalities, to a clear picture of spastic paraparesis.[docksci.com] Claypool Frontiers in Cell and Developmental Biology (2019) The genetic nomenclature of recessive cerebellar ataxias Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine[nature.com] Further symptoms comprise intolerance of protein-rich food, ataxia and spasticity, mood swings and behavioral problems.[symptoma.com]

  • Hallervorden-Spatz Syndrome

    Described features include 9,11 : progressive dementia extrapyramidal signs (rigidity, dystonia, choreoathetosis) corticospinal signs (spasticity, hyperreflexia) dysarthria[radiopaedia.org] The patient presented with a slowly progressive illness with seizures, extrapyramidal symptoms, cerebellar ataxia, dementia, spasticity, myoclonic movements and a severe demyelinating[ncbi.nlm.nih.gov] Additionally, affected individuals may experience a loss of intellectual function (dementia) and psychiatric symptoms such as behavioral problems, personality changes, and[ghr.nlm.nih.gov]

  • Familial Infantile Myoclonic Epilepsy

    Conclusions: XMESID is a rare X-linked recessive myoclonic epilepsy with spasticity and intellectual disability in boys. Hyperreflexia is found in carrier women.[neurology.org] Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias; Metabolic Disorders; Friedreich Ataxia; ALS; Dementia; Neuromuscular[books.google.de] problems sees the neurologist as recommended It's important to keep your child safe during a seizure.[kidshealth.org]

  • Cerebral Palsy

    Spastic features included hypertonicity, hyperreflexia, and extensor plantar responses. Two older sibs had contractures.[ncbi.nlm.nih.gov] BACKGROUND: Ataxia-telangiectasia (A-T) is an autosomal recessive disease that consists of progressive cerebellar ataxia, variable immunodeficiency, sinopulmonary infections[ncbi.nlm.nih.gov] Some behavioral problems are extreme irritability, feeding difficulties, persistent gagging or choking when fed after 6 months of age especially if the tongue pushes the food[web.archive.org]

  • Autosomal Recessive Spastic Paraplegia Type 39

    Neurological examination also showed the classic spastic paraplegia symptoms such as proximal weakness of the lower limbs and profound proximal spasticity.[omicsonline.org] Ataxia without neuropathy ( Pure cerebellar ataxia, possibly associated with other symptoms ) ARCA1 (610743) Late onset: 32 y (17–46 y) Pure cerebellar ataxia, late onset,[neupsykey.com] Another five patients had behavioral problems in childhood. Brain MRIs from nine patients were available for review.[nature.com]

  • Autosomal Recessive Spastic Paraplegia Type 46

    Affiliated tissues include brain , and related phenotypes are nystagmus and hyperreflexia Disease Ontology : 12 A hereditary spastic paraplegia that has material basis in[malacards.org] Another five patients had behavioral problems in childhood. Brain MRIs from nine patients were available for review.[nature.com] Neurological examination also showed the classic spastic paraplegia symptoms such as proximal weakness of the lower limbs and profound proximal spasticity.[omicsonline.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] G11.0 Congenital nonprogressive ataxia G11.1 Early-onset cerebellar ataxia G11.2 Late-onset cerebellar ataxia G11.3 Cerebellar ataxia with defective DNA repair G11.4 Hereditary[icd10data.com] Behavior problems are common having features of ADHD, autism, and aggression. Foot deformities have been noted.[disorders.eyes.arizona.edu]

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