Results 1 - 7 of 7 for Infantile GM1 gangliosidosis
  1. Genetics Home Reference: GM1 gangliosidosis From the National Institutes of Health (National Library of Medicine)  
    ... Registry: Gangliosidosis GM1 type 3 Genetic Testing Registry: Infantile GM1 gangliosidosis Genetic Testing Registry: Juvenile GM>1< gangliosidosis You ...
  2. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... from cardiac complications or pneumonia . Onset of late infantile GM1 gangliosidosis is typically between ages 1 and 3 years. ...
  3. Oculomotor Apraxia (American Association for Pediatric Ophthalmology and Strabismus)  
    ... Krabbe’s leucodystrophy, Pelizaeus Merzbacher disease, Infantile Gaucher disease, GM1 gangliosidosis, Infantile Refsum’s disease, propionic academia, ataxia telangiectasia, Bardet-Biedl ...
  4. Gangliosidoses From the National Institutes of Health (National Institute of Neurological Disorders and Stroke) - Short Summary  
    ... and blind by age 1. Onset of late infantile GM1 gangliosidosisis typically between ages 1 and 3 years. Signs include ataxia, seizures, dementia, and difficulties with speech. Adult GM1 gangliosidosis strikes between ages 3 and 30, with symptoms ...
  5. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Disease Network Aspartylglucosaminuria Batten disease Batten disease: late infantile Bone Disease in the MPS Cystinosis Danon disease Fabry Disease Farber disease Fucosidosis GM1-Gangliosidosis types I/II/III GM2-Gangliosidosis Galactosialidosis types ...
  6. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... Adult Fanconi syndrome - See Fanconi renotubular syndrome * Adult GM1 gangliosidosis - See GM1 gangliosidosis type 3 * Adult granulosa cell tumor of the ... See Adult-onset vitelliform macular dystrophy * Adult-onset GM1 gangliosidosis - See GM1 gangliosidosis type 3 * Adult-onset immunodeficiency ...
  7. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
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