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19 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Muscular Atrophy, Pyramidal Tract Signs

  • Amyotrophic Lateral Sclerosis

    Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?[ncbi.nlm.nih.gov] The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Upper Motor Neuron Disease

    Increased deep tendon reflex (DTR) Pronator drift [3] Corticospinal/pyramidal tract [ edit ] These are the neural tracts which descend in the ventral horn of the spinal cord[en.wikipedia.org] atrophy(PMA), Progressive bulbar palsy(PBP), MEPs were recorded from abductor pollicis brevis and abductor hallucis.[e-acn.org] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com]

  • Progressive Muscular Atrophy

    tract.[ncbi.nlm.nih.gov] The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[en.wikipedia.org] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?[ncbi.nlm.nih.gov] […] are not associated with a defect in the SMN1 gene on chromosome 5q X-linked spinal muscular atrophy X-linked spinal muscular atrophy is seen only among males![amboss.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Spinal Muscular Atrophy with Respiratory Distress Type 1

    ., et al. (2002) Autosomal dominant juvenile ALS and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?[doi.org] Homepage Rare diseases Search Search for a rare disease Spinal muscular atrophy with respiratory distress type 1 Disease definition Spinal muscular atrophy with respiratory[orpha.net] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Sensory abnormalities and pyramidal tract signs were absent in all cases, as was pes cavus.[nature.com] Treatment for spinal muscular atrophy Unfortunately, there is currently no specific treatment for SMA.[betterhealth.vic.gov.au] weakness DHMN8 600175 TRPV4 12q24.11 Autosomal dominant Congenital distal spinal muscular atrophy Affects primarily distal muscles of lower limbs, non-progressive, rare DHMNJ[en.wikipedia.org]

  • Distal Hereditary Motor Neuropathy Type 1

    Sensory abnormalities and pyramidal tract signs were absent in all cases, as was pes cavus.[nature.com] muscular atrophy, but have different genetic causes.[togetherinsma.com] weakness DHMN8 600175 TRPV4 12q24.11 Autosomal dominant Congenital distal spinal muscular atrophy Affects primarily distal muscles of lower limbs, non-progressive, rare DHMNJ[en.wikipedia.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?[sydney.edu.au] Homepage Rare diseases Search Search for a rare disease X-linked distal spinal muscular atrophy type 3 Disease definition X-linked distal spinal muscular atrophy type 3 is[orpha.net] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Distal Hereditary Motor Neuropathy

    Sensory abnormalities and pyramidal tract signs were absent in all cases, as was pes cavus.[nature.com] atrophy, distal, Charcot-Marie-Tooth disease AR 52 128 LAS1L * Spinal muscular atrophy with respiratory distress XL 5 4 PLEKHG5 Spinal muscular atrophy, Charcot-Marie-Tooth[blueprintgenetics.com] facial weakness and muscle atrophy in the hands ( 2 – 4 ).[spandidos-publications.com]

  • Lower Motor Neuron Syndrome with Late-Adult Onset

    A midline lesion of the medulla oblongata is likely to involve the pyramidal tracts (the descending motor pathway) and the medial lemnisci (the ascending tracts relaying sensory[britannica.com] muscular atrophy, but have different genetic causes.[togetherinsma.com] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com]

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