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14 Possible Causes for Inability to Supinate Forearm, Spastic Paralysis

  • Upper Motor Neuron Disease

    There are also rare progressive, autosomal recessive upper motor neuron degenerations (Infantile –Onset Ascending Hereditary Spastic Paralysis, Juvenile Primary Lateral Sclerosis[neuropathology-web.org] Dysdiadochokinesia refers to the inability of cerebellar patients to perform rapidly alternating movements, such as rapidly pronating and supinating the hands and forearms[nba.uth.tmc.edu] Signs: Upper Motor Neuron Lesion findings Muscle group weakness (not complete paralysis) Minimal muscle atrophy "Clasp-knife" spasticity Initial resistance to motion is strongest[fpnotebook.com]

  • Autosomal Dominant Spastic Paraplegia Type 9A

    […] paraplegia 53 AR 1 WDR48 612167 0 ZFYVE26 612012 spastic paraplegia type 15 AR 64 ALS2 606352 amyotrophic lateral sclerosis 2; Spastic paralysis, infantile onset ascending[centogene.com] Dysdiadochokinesia refers to the inability of cerebellar patients to perform rapidly alternating movements, such as rapidly pronating and supinating the hands and forearms[nba.uth.tmc.edu] Eymard‐Pierre E, Lesca G and Dollet S (2002) Infantile‐onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.[els.net]

  • Polyglucosan Body Myopathy Type 2

    paralysis AR 33 68 ANG Amyotrophic lateral sclerosis AD 8 37 ATL1 Spastic paraplegia, Neuropathy, hereditary sensory AD 29 84 BSCL2 Lipodystrophy, congenital generalized,[blueprintgenetics.com] Inability to do push-ups.[sites.google.com] paralysis, infantile onset ascending (IAHSP) Neurological Spastic paraplegia, autosomal dominant Neurological Spastic paraplegia, autosomal recessive Neurological Spastic[genomediagnosticsnijmegen.nl]

  • Distal Myopathy Type 3

    paralysis Intellectual deficit, X-linked, Turner type Joubert syndrome with renal defect Juvenile amyotrophic lateral sclerosis Juvenile primary lateral sclerosis LEOPARD[csbg.cnb.csic.es] Inability to do push-ups.[sites.google.com] The clinical phenotype of PLS can include gradual progressive leg weakness and spasticity and spastic bulbar weakness.[mayomedicallaboratories.com]

  • Hereditary Cerebellar Degeneration

    Spastic quadraparesis 2. Marked cerebellar ataxia 3. Spastic and ataxic dysarthria 4. Global supranuclear paralysis of vertical gaze 5.[collections.lib.utah.edu] This could involve rapidly switching from pronation to supination of the forearm.[en.wikipedia.org] Family spastic paralysis associated with amyotrophy. Rev. Neurol. Psychiat 1905;3:257-263. 5. Labrisseau A, Vanasse M, Brochu P, Jasmin G.[collections.lib.utah.edu]

  • Pyramidal Tract Disorder

    Bilateral Corticospinal disfx spasticity, hyperreflexia, Babinski Anterior Horn Cell Syndrome FDR, LMN Disorder Weakness, flaccid paralysis, atrophy, and fasciculations, reduced[memorize.com] Dysdiadochokinesia refers to the inability of cerebellar patients to perform rapidly alternating movements, such as rapidly pronating and supinating the hands and forearms[nba.uth.tmc.edu] Unconsciousness and spastic paralysis of the limbs are the primary symptoms.[britannica.com]

  • Brain Stem Disorder

    Unconsciousness and spastic paralysis of the limbs are the primary symptoms.[britannica.com] Dysdiadochokinesia refers to the inability of cerebellar patients to perform rapidly alternating movements, such as rapidly pronating and supinating the hands and forearms[nba.uth.tmc.edu]

  • Autosomal Dominant Myoglobinuria

    Diffuse myelin abnormalities in infants produce retardation of motor development, spastic paralysis. C. NUTRITIONAL, TOXIC AND METABOLIC DISORDERS 1.[therapyedu.com] Inability to do push-ups.[sites.google.com] […] recessive AFG3L2 Spastic paralysis, infantile onset ascending ALS2 Spastic paraplegia type 74, autosomal recessive IBA57 Spastic paraplegia type 74, autosomal recessive IBA57[centogene.com]

  • Antenatal-Onset Multicore Myopathy with Arthrogryposis

    Paralysis, Infantile-onset Spastic Paraplegia Spastic Paraplegia 3 Spastic Paraplegia 10 Spastic Paraplegia, Autosomal Dominant Spherocytosis, Hereditary Spherocytosis, Hereditary[sequencing.com] Inability to do push-ups.[sites.google.com] paralysis Agammaglobulinemia, microcephaly, and severe dermatitis Renal hypouricemia Microcephaly sparse hair mental retardation seizures Dentinogenesis imperfecta type 2[checkrare.com]

  • Dysdiadochokinesis

    Impaired vibratory sensation ; Limb ataxia ; Muscle cramps ; Myoclonus ; Neurodegeneration ; Oculomotor apraxia ; Olivopontocerebellar atrophy ; Ophthalmoplegia ; Pain ; Paralysis[genedx.com] It is most readily demonstrated by asking the patient to pronate and supinate an arm at speed, with a tap on the opposite forearm at the extremes of movement.[gpnotebook.co.uk] […] instability ; Postural tremor ; Progressive cerebellar ataxia ; Respiratory failure ; Rigidity ; Rod-cone dystrophy ; Skeletal muscle atrophy ; Slow saccadic eye movements ; Spasticity[genedx.com]

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