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Results 1 - 6 of 6 for "Dejerine-Sottas" disease
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  1. PMP22 gene 
    ... Charcot-Marie-Tooth disease sometimes referred to as Dejerine-Sottas disease or type 3 Charcot-Marie-Tooth disease. This ... causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype. Am J Med Genet A. 2008 Sep ...
    https://medlineplus.gov/genetics/gene/pmp22 - Genetics
  2. Charcot-Marie-Tooth disease 
    ... AND HEREDITARY MOTOR-SENSORY NEUROPATHY HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D HEREDITARY MOTOR AND SENSORY NEUROPATHY ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  3. TRPV4 gene 
    The TRPV4 gene provides instructions for making a protein that acts as a calcium channel. This channel, which transports positively charged atoms of calcium ( ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  4. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF ... muscular dystrophy; exercise with a disability; neuromuscular ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  5. Charcot-Marie-Tooth Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Charcot-Marie-Tooth Disease/Start Here ... Charcot-Marie-Tooth Disease ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of ...
    https://www.ninds.nih.gov/.../disorders/charcot-marie-tooth-disease - External Health Links
  6. MPZ gene 
    ... as walking. This form of Charcot-Marie-Tooth disease is sometimes called Dejerine-Sottas syndrome, congenital hypomyelination, or Roussy-Levy syndrome. Researchers ...
    https://medlineplus.gov/genetics/gene/mpz - Genetics