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115 Possible Causes for Hyperreflexia, Spasticity - Hyperreflexia, Upper Limbs May Be Affected

  • 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] Neurologic examination revealed hyperreflexia and spasticity in the lower extremities, weakness of hip flexion and ankle dorsiflexion, extensor plantar response, diminished[neurology.org] […] in upper limbs 0007350 Impaired proprioception 0010831 Lower limb hyperreflexia Overactive lower leg reflex 0002395 Pes cavus High-arched foot 0001761 Proximal lower limb[rarediseases.info.nih.gov]

  • 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] SPG39 is associated with a motor axonopathy affecting upper and lower limbs and resulting in progressive wasting of distal upper and lower extremity muscles.[mybiosource.com] ) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by varying degrees of lower limb spasticity, pyramidal weakness, hyperreflexia[medicbind.com]

  • 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] Both types involve the lower limbs; the complex types may also involve the upper limbs, although to a lesser degree.[ghr.nlm.nih.gov] […] drugs.Orpha Number: 100998Disease definitionA complex hereditary spastic paraplegia characterized by progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia[malacards.org]

  • 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] In SPG56, upper limbs are often also affected. Some SPG56 patients may have a subclinical axonal neuropathy. {ECO:0000269 PubMed:23176821}.[genecards.org] The gait is spastic with weakness, hyperreflexia, and extensor plantar responses in the lower limbs. The upper limbs are variably involved and movements are dysmetric.[disorders.eyes.arizona.edu]

  • Autosomal Dominant Spastic Paraplegia Type 29

    24, Autosomal Recessive Symptoms via clinical synopsis from OMIM: 57 Neurologic Central Nervous System: spasticity hyperreflexia clonus difficulty standing walking on tiptoes[malacards.org] In SPG56, upper limbs are often also affected. Some SPG56 patients may have a subclinical axonal neuropathy.[malacards.org] […] and phenotypes: Commonly - More than 50% cases Genetic anticipation Not very common - Between 30% and 50% cases Neonatal hyperbilirubinemia Commonly - More than 50% cases Hyperreflexia[mendelian.co]

  • Upper Motor Neuron Disease

    No spasticity or hyperreflexia.[brainscape.com] Progressive bulbar palsy (PBP) Affects about a quarter of people diagnosed, and involves both the upper and lower motor neurones .[bournemouthphysiotherapy.co.uk] Examination reveals UMN signs in the legs (weakness, spasticity, pathological reflexes, hyperreflexia), although reflexes may also be brisk in the arms.[clinicalgate.com]

  • Spastic Paraplegia

    This case showed spasticity and hyperreflexia with pathological reflexes and ankle clonus as well as muscle weakness in all extremities.[ncbi.nlm.nih.gov] A trace of terminal dysmetria may sometimes found in the upper limbs However affected individuals do not show more florid cerebellar signs..[medicaljoyworks.com] On neurological examination, he showed hyperreflexia, spasticity, and weakness in the lower extremities and bilateral Babinski reflexes.[ncbi.nlm.nih.gov]

  • Amyotrophic Lateral Sclerosis Type 1

    hyperreflexia ( ) Hoffman's ( ) Babinski's spastic dysarthria lower motor neuron (LMN) signs muscular atrophy weakness clinical fasciculations clumsiness Evaluation Diagnosis[orthobullets.com] […] and manual dexterity (in upper limb involvement).[aafp.org] Clinical manifestations include progressive weakness, atrophy, fasciculation, hyperreflexia, dysarthria, dysphagia, and eventual paralysis of respiratory function.[icd10data.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] Both types involve the lower limbs; the complex types may also involve the upper limbs, although to a lesser degree.[icdlist.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]

  • Multifocal Motor Neuropathy

    Upper motor neuron signs (spasticity, hyperreflexia, extensor plantar response).[clinicaltrials.gov] Upper limbs are usually primarily and more severely affected, but lower limbs may be involved during the course of the disease.[ncbi.nlm.nih.gov] Atrophy may be present, but hyperreflexia and spasticity are not seen.[ncbi.nlm.nih.gov]

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