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Results 1 - 6 of 6 for Spinal muscular "atrophy," lower "extremity," autosomal dominant
  1. Genetics Home Reference: Spinal muscular atrophy From the National Institutes of Health (National Library of Medicine)  
    ... Testing Registry: Kugelberg-Welander disease Genetic Testing Registry: Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Genetic Testing Registry: Spinal muscular atrophy, type II ...
  2. Motor Neuron Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... disease of the upper motor neurons, while progressive muscular atrophy affects only ... Autosomal dominant means that a person needs to inherit only ...
  3. Muscular Dystrophy: Hope Through Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... is X-linked recessive and the other is autosomal dominant. Onset ... and symmetric weakness. Contractures in the spine, ankles, ...
  4. Charcot-Marie-Tooth Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... of motor nerves results in muscle weakness and atrophy in the extremities (arms, ... in an autosomal dominant fashion, which means that only one copy of ...
  5. Charcot-Marie-Tooth and Related Diseases (Muscular Dystrophy Association) - PDF  
    ... information about the feet and hands to the spinal cord and then the brain, so that ... the lower legs, the hands and the forearms. Although CMT ...
  6. ... Neuron Diseases Amyotrophic lateral sclerosis (ALS) Infantile progressive spinal muscular atrophy (Type 1, Werdnig-Hoffmann disease) Intermediate spinal muscular ...