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64 Possible Causes for Non-Communicating, Isolated Syringomyelia

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  • Arnold-Chiari Malformation Type 1

    It consists of a downward displacement of the cerebellar tonsils through the foramen magnum (the opening at the base of the skull), sometimes causing non-communicating hydrocephalus[disabled-world.com] […] of the posterior fossa, and 3) isolation and analysis of genomic DNA from whole blood for linkage analysis.[clinicaltrials.gov] Design: Human subjects will undergo 1) neurologic examinations, 2) head and cervical MRI scans to evaluate for the Chiari I malformation, syringomyelia, and maldevelopment[clinicaltrials.gov]

  • Syringobulbia

    It can be accompanied by syringomyelia either communicating or non- communicating with it [11].[beat-journal.com] syringomyelia.[ncbi.nlm.nih.gov] At times this is referred to as, 'non-communicating syringomyelia.'[disabled-world.com]

  • Syringomyelia

    At times this is referred to as, 'non-communicating syringomyelia.'[disabled-world.com] H. 2018 7 Resolution of isolated syringomyelia after removing thoracic disc herniation. ( 29316818 ) El Ouadih Y....Chaix R. 2018 8 Unilateral hyperhidrosis as persistently[malacards.org] "Non-communicating" syringomyelia: a non-existent entity. Surg Neurol 1976;6:251-256. [ Links ] 15. Williams B.[scielo.br]

  • Familial Recurrent Peripheral Facial Palsy

    […] myopathy with cores Congenital myopathy with excess of thin filaments Congenital myopathy, Paradas type Congenital myotonia Congenital neuronal ceroid lipofuscinosis Congenital non-communicating[se-atlas.de] […] and an ear nose and throat doc who says I have non-motor Bell’s Palsy (my research indicates there is no such thing).”[hnppwellbeing.com] Familial exudative vitreoretinopathy Familial focal epilepsy with variable foci Familial infantile bilateral striatal necrosis Familial infantile myoclonic epilepsy Familial isolated[se-atlas.de]

  • Multi-Infarct Dementia

    NEUROLOGY 1997;48: 668-672 Copyright 1997 by Advanstar Communications Inc.[neurology.org] Isolated increases of GFAp could be demonstrated in patients with dementia (Alzheimer type or multi-infarct dementia ) or syringomyelia [27].[wikigenes.org] Community and hospital care Patients should be cared for in the community as much as possible.[patient.info]

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    […] myopathy with cores Congenital myopathy with excess of thin filaments Congenital myopathy, Paradas type Congenital myotonia Congenital neuronal ceroid lipofuscinosis Congenital non-communicating[se-atlas.de] Familial exudative vitreoretinopathy Familial focal epilepsy with variable foci Familial infantile bilateral striatal necrosis Familial infantile myoclonic epilepsy Familial isolated[se-atlas.de] […] seizures Familial or sporadic hemiplegic migraine Familial paroxysmal ataxia Familial partial epilepsy Familial porencephaly Familial recurrent peripheral facial palsy Familial syringomyelia[se-atlas.de]

  • Distal Hereditary Motor Neuropathy Type 1

    […] myopathy with cores Congenital myopathy with excess of thin filaments Congenital myopathy, Paradas type Congenital myotonia Congenital neuronal ceroid lipofuscinosis Congenital non-communicating[se-atlas.de] Familial exudative vitreoretinopathy Familial focal epilepsy with variable foci Familial infantile bilateral striatal necrosis Familial infantile myoclonic epilepsy Familial isolated[se-atlas.de] […] seizures Familial or sporadic hemiplegic migraine Familial paroxysmal ataxia Familial partial epilepsy Familial porencephaly Familial recurrent peripheral facial palsy Familial syringomyelia[se-atlas.de]

  • Arnold-Chiari Malformation Type 2

    There are two types of hydrocephalus: communicating (or non-obstructive) and non-communicating (obstructive).[hawaii.edu] CM-I; 16 of them (53%) had syringomyelia.[doi.org] […] of the posterior fossa, and 3) isolation and analysis of genomic DNA from whole blood for linkage analysis.[clinicaltrials.gov]

  • Arnold Chiari Malformation

    The cystic lesion was histologically confirmed to be a non-communicated hydrocele of canal of Nuck.[ncbi.nlm.nih.gov] CM-I; 16 of them (53%) had syringomyelia.[doi.org] There are two types of hydrocephalus: communicating (or non-obstructive) and non-communicating (obstructive).[hawaii.edu]

  • Limb-Girdle Muscular Dystrophy Type 2J

    […] myopathy with cores Congenital myopathy with excess of thin filaments Congenital myopathy, Paradas type Congenital myotonia Congenital neuronal ceroid lipofuscinosis Congenital non-communicating[se-atlas.de] Most patients with LGMD2H belong to the isolated Hutterite community in Manitoba and have the D487N mutation.[emedicine.medscape.com] Familial exudative vitreoretinopathy Familial focal epilepsy with variable foci Familial infantile bilateral striatal necrosis Familial infantile myoclonic epilepsy Familial isolated[se-atlas.de]

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