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515 Possible Causes for Global Hypotonia, Multifocal Independent Spikes

  • West Syndrome

    A 5 year-old boy exhibited global hypotonia with generalized muscle weakness from birth.[] His MRI also picked up that his brain wasn't quite fully formed at the front and sides and this had resulted in him having global developmental delay and hypotonia (floppy[]

  • Generalized Clonic or Tonic-Clonic Seizures

    […] developmental delay Generalized hypotonia SOURCES: ORPHANET OMIM ICD10 NCIT MONDO More info about NIEMANN-PICK DISEASE, TYPE C1; NPC1 Top 5 symptoms//phenotypes associated[] […] seizures Pica Epileptic spasms EEG with irregular generalized spike and wave complexes Enhancement of the C-reflex Dysphagia Urinary bladder sphincter dysfunction Severe global[] Tetraplegia Neurodegeneration Spastic tetraplegia Epileptic encephalopathy Intellectual disability, profound Status epilepticus Hypoplasia of the corpus callosum Muscular hypotonia[]

  • Encephalopathy

    We describe a multiplex consanguineous family in which four affected members presented with severe neonatal hypotonia, profound global developmental delay, progressive microcephaly[] Global developmental delay can be evident by this age or the patients may present with encephalopathy or hypotonia. 2 , 7 , 8 Classification by age of onset into an early[]

  • Epilepsy

    Epilepsy is a heterogeneous disorder, the symptoms of which are preventable and controllable to some extent. Significant inter- and intra-country differences in incidence and prevalence exist because multiple etiologic factors are implicated. Many past reviews have addressed sole etiologies. We considered a[…][]

    Missing: Global Hypotonia
  • Myoclonic-Astatic Epilepsy

    In a clinical setting, the occurrence of periodic clusters and independent focal or multifocal accentuations of generalized spike-and-wave complexes in interictal EEG may[]

    Missing: Global Hypotonia
  • Benign Adult Familial Myoclonic Epilepsy

    Abstract Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by cortical tremor and generalized seizures, mapped on chromosome 8q24 by Japanese authors. Recently the same phenotype also was reported in European families, with linkage on chromosome 2. We present a new[…][]

    Missing: Global Hypotonia
  • Juvenile Myoclonic Epilepsy

    Delayed diagnosis of juvenile myoclonic epilepsy. R A Grünewald, E Chroni, C P Panayiotopoulos Department of Clinical Neurophysiology and Epilepsy, St Thomas' Hospital, London, UK. Abstract Fifteen cases of juvenile myoclonic epilepsy (JME) were identified from one hundred and eighty consecutive patients referred to a[…][]

    Missing: Global Hypotonia
  • Idiopathic Generalized Epilepsy

    The full text of this article hosted at is unavailable due to technical difficulties. First published: 18 November 2005 Cited by: 5 Address correspondence and reprint requests to Dr. Douglas R. Nordli, Jr., at Children's Memorial Hospital, Northwestern University, Feinberg School of Medicine, 2300 Children's[…][]

    Missing: Global Hypotonia
  • Organic Brain Syndrome

    This paper describes a rare case of organic brain syndrome with psychosis and clinically transverse myelopathy, as initial manifestations of systemic lupus erythematosus in an elderly woman. The identification and evaluation of antibodies to ribosome P in the serum and cerebrospinal fluid may be of help in such cases[…][]

    Missing: Global Hypotonia
  • Juvenile Absence Epilepsy

    To report three cases of juvenile absence epilepsy (JAE) with temporal intermittent, asynchronous delta activity over the temporal regions. Long term video-EEG using the international 10/20 system and supplementary anterior-inferior temporal electrodes. Cohort of 1123 patients included in our active file seen at[…][]

    Missing: Global Hypotonia

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