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1,990 Possible Causes for EMG Shows Neurogenic Abnormalities, Facial Muscle Weakness and Progressive Atrophy, No Sensory Deficit

  • Distal Hereditary Motor Neuropathy Type 2A

    An autosomal recessive neuromuscular disorder (OMIM:608634) caused by selective impairment of motor neurons in the anterior horn of the spinal cord, without sensory deficit[medical-dictionary.thefreedictionary.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] Sensory deficits affecting touch, pain, temperature, and vibration were present in the feet up to the knees and in both hands.[scielo.br]

  • Distal Hereditary Motor Neuropathy Type 2

    […] neuropathy (HMSN) : CMT (Charcot Marie Tooth) is a broad category with mild deficits such as clumsiness, distal motor weakness, classic "stork leg deformity" and possible[pathologyoutlines.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] Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1. Neurology. 1989 Oct. 39(10):1302-8.[emedicine.medscape.com]

  • Spinal Muscular Atrophy Type 4

    Neurological deficits are similar to that of other spinal cord lesions, with weakness, sphincter abnormalities and sensory changes. [11] Ependymomas tend to occur centrally[sjmms.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] Scapuloperoneal spinal muscular atrophy: Type 1 (AD form) appears at age 14-26, with weakness, distal leg atrophy, and absent tendon reflexes and sparing of intrinsic foot[emedicine.medscape.com]

  • 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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: No Sensory Deficit
  • Spinal Muscular Atrophy Type 1

    We present a baby with spinal muscular atrophy type 1, an inherited disorder causing progressive weakness, leading to complete paralysis of respiratory, facial and limb muscles[ncbi.nlm.nih.gov] 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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info]

    Missing: No Sensory Deficit
  • Spinal Muscular Atrophy Type 2

    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] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: No Sensory Deficit
  • Amyotrophic Lateral Sclerosis

    EMG change were at an earlier stage of evolution than those showing severe weakness and marked neurogenic EMG change.[doi.org] This can be suspected when additional neurological symptoms are present, such as cerebellar symptoms, seizures, or sensory deficits.[clinicaladvisor.com] In cranial nerves, common symptoms are atrophy of facial muscles and progressive bulbar palsy (PBP).[flexikon.doccheck.com]

  • Multifocal Motor Neuropathy

    A 49-year-old patient reported a history of slowly progressive predominantly distal tetraparesis, with mild sensory deficits.[ncbi.nlm.nih.gov] 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] Of note, sensory deficits are not typical of MMN.[symptoma.com]

    Missing: EMG Shows Neurogenic Abnormalities
  • Congenital Trigeminal Anesthesia

    deficit involving all or some of the sensory components of the trigeminal nerve.[orpha.net] 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] […] rare disease Congenital trigeminal anesthesia Disease definition Congenital trigeminal anesthesia is a rare neuro-ophtalmological disorder characterized by a congenital sensory[orpha.net]

    Missing: EMG Shows Neurogenic Abnormalities
  • Distal Hereditary Motor Neuropathy Type 2C

    deficit (posterior horn).[medical-dictionary.thefreedictionary.com] deficit in the posterior horn.[uniprot.org] […] neuropathy (HMSN) : CMT (Charcot Marie Tooth) is a broad category with mild deficits such as clumsiness, distal motor weakness, classic "stork leg deformity" and possible[pathologyoutlines.com]

    Missing: Facial Muscle Weakness and Progressive Atrophy

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