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Results 1 - 5 of 5 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. 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 ...
  4. 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 ...
  5. 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. ...