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62 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Sensation Normal

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    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] DSMA4 is characterized by childhood onset, generalized muscle weakness and atrophy with denervation and normal sensation. Bulbar symptoms and pyramidal signs are absent.[uniprot.org] Clinically, AMAN is part of the GBS spectrum but distinguished by normal sensation and nerve conduction studies characterised by low distal motor evoked amplitudes, normal[jnnp.bmj.com]

  • Upper Motor Neuron Disease

    Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com] Reflexes were normal on the right. On the left, the reflexes were brisk. Sensation was normal.[oxfordmedicaleducation.com] […] was normal Coordination was in proportion to the weakness Eye movements were normal To complete my examination I would like to: perform full upper limb neurological examination[medicaleducationleeds.com]

  • Multifocal Motor Neuropathy

    In the first patient the symptoms were slowly progressive with bulbar muscle impairment, generalized weakness, muscular atrophy with cramps and fasciculations.[moh-it.pure.elsevier.com] Sensation was normal and reflexes were reduced asymmetrically.[ncbi.nlm.nih.gov] Sensation was normal, and reflexes were reduced asymmetrically.[ncbi.nlm.nih.gov]

  • Progressive Muscular Atrophy

    Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Muscle tone was normal. Cranial nerves were normal. Tendon reflexes were absent at the right ankle, but 2 elsewhere. Sensation was normal.[neuromuscular.wustl.edu] 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 and Bulbar Muscular Atrophy

    Abstract Spinal and bulbar muscular atrophy (SBMA) is the first member identified among polyglutamine diseases characterized by slowly progressive muscle weakness and atrophy[ncbi.nlm.nih.gov] Development of sensations and the mind are completely normal in SMA. Type 1 Type 1 SMA is the most severe, affecting children under the age of 2.[verywell.com] The main symptoms are slowly progressive muscle weakness and atrophy of bulbar, facial and limb muscles.[ncbi.nlm.nih.gov]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    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] Localization to the motor neuron is suspected when the clinical picture demonstrates distal weakness and atrophy with normal sensation.[clinicalgate.com] sensation and equivalent degrees of injury.[care.diabetesjournals.org]

  • Distal Spinal Muscular Atrophy Type 3

    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]  Loss of function of spinal motor neurons causing progressive weakness of muscles Muscles include extremities, respiratory muscles Sensation is normal Brain function is[slideshare.net] sensation SMA-3 Proximal weakness and hypotonia Gait: Trendelenburg, hyperlordosis, may walk on toes as compensatory maneuver to promote knee extension Positive Gower sign[now.aapmr.org]

  • Myositis

    Muscular dystrophies are associated with presentation in childhood or adolescence, a slowly progressive course, early muscle atrophy, involvement of the facial muscles, a[rheumatologyadvisor.com] Muscular atrophy occurs with preservation of tendon reflexes, flexor plantar response and normal sensation.[patient.info] […] family history of muscle weakness, calf atrophy or hypertrophy, and early distal muscle weakness.[rheumatologyadvisor.com]

  • Ophthalmic Nerve Disorder

    The distinguishing clinical features of the disease include slowly progressive proximal greater than distal limb weakness, bulbar weakness involving primarily facial and tongue[neupsykey.com] This can lead to attacks of pain caused by the misdirection of signals sub-serving normal painless sensation.[ansdocs.com] All modalities of sensation were preserved in the ophthalmic nerve division (V1). Corneal reflexes were normal.[jnnp.bmj.com]

  • Distal Hereditary Motor Neuropathy Type 1

    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] Strength of other muscle groups was intact and all modalities of sensation were normal.[journals.plos.org] These normally painful conditions do not hurt because of the loss of sensation.[rarediseases.org]

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