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Results 1 - 10 of 24 for Lower limb amyotrophy
Did you mean Lower limb amyotrophic?
  1. ... atrophy, juvenile, proximal, autosomal dominant Spinal muscular atrophy, lower extremity, autosomal dominant Spinal muscular atrophy, lower extremity, dominant Genetic Testing Registry: Autosomal dominant ...
  2. ... movement (motor neuropathy); exaggerated reflexes (hyperreflexia) of the lower limbs; muscle wasting (amyotrophy); or reduced bladder control. Rarely, spastic paraplegia type ...
  3. Spinal Muscular Atrophy (National Library of Medicine)  
    What is spinal muscular atrophy (SMA)? Spinal muscular atrophy (SMA) is a group of genetic diseases that damages and kills motor neurons. Motor neurons ...
  4. ... with progressive myoclonic epilepsy, spinal muscular atrophy with lower extremity predominance, X-linked infantile spinal muscular atrophy, and spinal muscular atrophy with respiratory distress type ...
  5. Describing SMA (Cure SMA)  
    Spinal Muscular Atrophy/Start Here ... Spinal Muscular Atrophy ... Cure SMA ... Make today a breakthrough. No two people with spinal muscular atrophy (SMA) have identical ...
  6. ... BICD2 gene have been found to cause spinal muscular atrophy with lower extremity predominance (SMA-LED). This condition is characterized by ...
  7. ... of their limbs or detect vibrations with their lower limbs. They may also have muscle wasting (amyotrophy), reduced bladder control, or high arches of the ...
  8. ... type 3A can also experience progressive muscle wasting (amyotrophy) in the lower limbs, reduced bladder control, an abnormal curvature of the ...
  9. ... type 31 can also experience progressive muscle wasting (amyotrophy) in the lower limbs, exaggerated reflexes (hyperreflexia), a decreased ability to feel ...
  10. ... neuropathy); intellectual disability; exaggerated reflexes (hyperreflexia) of the lower limbs; speech difficulties (dysarthria); reduced bladder control; and muscle wasting (amyotrophy). Less common features include difficulty swallowing (dysphagia), high- ...
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