Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 4 of 4 for "Dejerine-Sottas" disease
Did you mean "determine-scott" disease?
  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, DEMYELINATING, TYPE 4D; CMT4D HEREDITARY MOTOR AND SENSORY ...
    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. 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