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Results 31 - 40 of 68 for Progressive muscular dystrophy
  1. LAMA2 gene 
    ... have been identified in individuals with LAMA2-related muscular dystrophy, a disorder that causes weakness and wasting (atrophy) ... gene mutations that cause early-onset LAMA2-related muscular dystrophy result in the absence of functional laminin alpha- ...
    https://medlineplus.gov/genetics/gene/lama2 - Genetics
  2. ANO5 gene 
    ... have been identified in people with limb-girdle muscular dystrophy type 2L. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/ano5 - Genetics
  3. SGCB gene 
    ... have been identified in people with limb-girdle muscular dystrophy type 2E. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/sgcb - Genetics
  4. SGCD gene 
    ... have been identified in people with limb-girdle muscular dystrophy type 2F. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/sgcd - Genetics
  5. SGCA gene 
    ... have been identified in people with limb-girdle muscular dystrophy type 2D. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/sgca - Genetics
  6. FKTN gene 
    ... gene have been found to cause Fukuyama congenital muscular dystrophy, a condition that affects the development of the ... brain, and skeletal muscles. This form of congenital muscular dystrophy occurs primarily in people of Japanese ancestry. Most ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  7. FKRP gene 
    ... of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  8. Chromosome 4 
    ... or number of copies of chromosome 4. Facioscapulohumeral muscular dystrophy is caused by genetic changes in the long ( ... wasting (atrophy) that worsens slowly over time. Facioscapulohumeral muscular dystrophy is a result of changes in a region ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics
  9. SGCG gene 
    ... have been identified in people with limb-girdle muscular dystrophy type 2C. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/sgcg - Genetics
  10. LMNA gene 
    ... have been identified in people with Emery-Dreifuss muscular dystrophy, a condition that affects muscles used for movement ( ... the LMNA gene mutations that cause Emery-Dreifuss muscular dystrophy change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
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