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28 Possible Causes for Generalized Dystonia, Homonymous Hemianopsia, Myopathy

  • MELAS Syndrome

    Deschauer et al. 2007 described a patient presenting with occipital seizures and residual homonymous hemianopsia, headache and ataxia and carrying two heterozygous POLG1 mutations[] ; alternating with ataxia, dystonia, choreoathetosis and spastic paraplegia.[] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[]

  • Occipital Lobe Tumor

    Clinical significance [ edit ] If one occipital lobe is damaged, the result can be homonymous hemianopsia vision loss from similarly positioned "field cuts" in each eye.[] Movement Disorders Patients with movement disorders, such as Parkinson’s disease, dystonia and essential tremor, are generally treated by Deep Brain Stimulation (DBS) after[] Complications of Dexamethasone, Continued Psychosis Hallucinations Hiccups Dementia Seizures Dependence Epidural lipomatosis Complications of Dexamethasone: Steroid myopathy[]

  • Lethal Infantile Mitochondrial Myopathy

    hemianopsia, right hemiparesis, language problems Workup: Serum lactic acidosis MRI 26 Diagnosis?[] […] avoid dantrolene if liver is involved). • Dystonia (diazepam, botulinum toxin [focal], trihexyphenidyl). • Headache (acute: nonsteroidal anti-inflammatory drugs and acetaminophen[] LEVIM stands for "Lethal Infantile Mitochondrial Myopathy" How to abbreviate Lethal Infantile Mitochondrial Myopathy?[]

  • Spastic Ataxia with Congenital Miosis

    Contralateral homonymous hemianopsia (compress ipsilateral PCA) 4.[] […] syndrome Friedreich ataxia Frontotemporal dementia with motor neuron disease Frontotemporal neurodegeneration with movement disorder Fucosidosis GM1 gangliosidosis type 2 Generalized[] E-2529 149 Metabolic Myopathies E-2547 150 Inflammatory Myopathies E-2595 151 Channelopathies E-2605 152 Management of Children with Neuromuscular Disorders E-2626 153 Endocrine[]

  • Scapuloperoneal Spinal Muscular Atrophy

    82 333 291, 366, 379, 381 heteronymous 82 Hering–Breuer reflex 150 acute 162, 290 homonymous, altitudinal 82 Herniation brain edema 162–163 Hemiballism 66–67 intervertebral[] Severe limb deficit Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome Severe motor and intellectual disabilities-sensorineural deafness-dystonia[] […] and scapulo-peroneal myopathy.[]

  • Spastic Quadriplegic Cerebral Palsy Type 2

    Field Defects - Field defects, especially homonymous hemianopsia and variants, are seen in hemiplegic CP.[] With significant dystonia/involuntary movements Dystonia and involuntary movements (specifically choreoathetosis) are not as common in CP as is generally believed.[] Diseases related with Myopathy and Spastic tetraplegia In the following list you will find some of the most common rare diseases related to Myopathy and Spastic tetraplegia[]

  • Deafness - Opticoacoustic Nerve Atrophy - Dementia Syndrome

    […] tunnel vision -psych problem Deficit: blindness in left eye Lesion: Deficit: bitemporal heteronymous hemianopsia Deficit: binasal heteronymous hemianopsia Right homonymous[] Rapidly progressive generalized dystonia in deafness-dystonia syndrome with cochlear implant and response to pallidal deep brain stimulation.[] Mitochondrial myopathy with lactic acidosis 0 *Acidosis, Lactic *Growth Disorders *Hearing Loss, Central *Mitochondrial Myopathies.[]

  • Ischemic Peripheral Neuropathy

    hemianopsia).[] Generalized dystonia (e.g., dystonia musculorum deformans) is an inherited condition in which persistent and often painful twisting and writhing movements of any muscle group[] Few cases of acute or chronic inflammatory demyelinating polyradiculoneuropathy were reported. ( 35 ) Generally, myopathies in SLE take the form of inflammatory myopathies[]

  • Familial Hypertryptophanemia

    Homonymous hemianopsia 402. Horizontal gaze palsy 403. Horner’s syndrome 404. Horror fusionis 405. Hunter syndrome 406. Hurler syndrome 407. Hurler–Scheie syndrome 408.[] […] polymicrogyria Early infantile epileptic encephalopathy 25 Duane syndrome type 1 Glycogen storage disease type 12 Rapid-onset dystonia-parkinsonism Limb-girdle muscular dystrophy[] […] acidosis and sideroblastic anemia Myopathy with lysis of myofibrils Myopathy, centronuclear Myopathy, desmin storage Myopathy, McArdle type Myopathy, myotubular Myopathy,[]

  • Infantile Hemiplegia

    Clinical features include contralateral weakness and loss of sensation in the arm and face and a contralateral homonymous hemianopsia.[] Other neurological manifestations include epilepsy, developmental delay, intellectual deficit, choreoathetosis, dystonia and ataxia.[] - CP norma- congential myopathies (?)[]

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