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Results 1 - 8 of 8 for Congenital hypomyelinating neuropathy
  1. Congenital Hypomyelinating Neuropathy (CHN) (Muscular Dystrophy Association)  
    ... Search form Search Charcot-Marie-Tooth Disease (CMT) Congenital Hypomyelinating Neuropathy (CHN) What is Congenital Hypomyelinating Neuropathy (CHN)? CHN ...
  2. Charcot-Marie-Tooth and Related Diseases (Muscular Dystrophy Association) - PDF  
    ... certain drugs and other potential causes of neuropathy. Congenital hypomyelinating neuropathy (CHN) Onset: congenital (at or near birth) Inheritance: autosomal recessive, spontaneous ...
  3. CMTX (Muscular Dystrophy Association)  
    ... CMT CMT1-CMT2 CMTX CMT4 Dejerine-Sottas disease Congenital Hypomyelinating Neuropathy (CHN) Signs and Symptoms Diagnosis Causes/Inheritance Medical ...
  4. CMT4 (Muscular Dystrophy Association)  
    ... CMT CMT1-CMT2 CMTX CMT4 Dejerine-Sottas disease Congenital Hypomyelinating Neuropathy (CHN) Signs and Symptoms Diagnosis Causes/Inheritance Medical ...
  5. CMT1-CMT2 (Muscular Dystrophy Association)  
    ... CMT CMT1-CMT2 CMTX CMT4 Dejerine-Sottas disease Congenital Hypomyelinating Neuropathy (CHN) Signs and Symptoms Diagnosis Causes/Inheritance Medical ...
  6. Dejerine-Sottas Disease (Muscular Dystrophy Association)  
    ... CMT CMT1-CMT2 CMTX CMT4 Dejerine-Sottas disease Congenital Hypomyelinating Neuropathy (CHN) Signs and Symptoms Diagnosis Causes/Inheritance Medical ...
  7. Charcot-Marie-Tooth Disease (National Library of Medicine)  
    Charcot-Marie-Tooth disease (CMT) is a group of genetic nerve disorders. It is named after the three doctors who first identified it. In the United States, CMT ...
  8. ... Marie-Tooth disease type 2P Genetic Testing Registry: Congenital hypomyelinating neuropathy Genetic Testing Registry: Dejerine-Sottas disease Genetic Testing ...