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Results 1 - 10 of 11 for Fukuyama congenital muscular dystrophy
  1. Fukuyama congenital muscular dystrophy 
    Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  2. Walker-Warburg syndrome 
    Walker-Warburg syndrome is an inherited disorder that affects development of the muscles, brain, and eyes. It is the most severe of a group of genetic conditions ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  3. FKTN gene 
    ... the FKTN gene have been found to cause Fukuyama congenital muscular dystrophy, a condition that causes skeletal muscle weakness and ... and function of skeletal muscles in people with Fukuyama congenital muscular dystrophy.Defective α-dystroglycan also affects the migration of ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  4. Muscular Dystrophy (National Library of Medicine)  
    ... slowly. It often starts in the teenage years. Congenital muscular dystrophies, which are present ... National Institute of Neurological Disorders and Stroke
    https://medlineplus.gov/musculardystrophy.html - Health Topics
  5. POMT1 gene 
    ... the POMT1 gene have been found to cause Walker-Warburg syndrome, the most severe form of a group of disorders known as congenital muscular dystrophies. Individuals with Walker-Warburg syndrome have skeletal muscle weakness and abnormalities of the ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
  6. CRPPA gene 
    ... the CRPPA gene have been found to cause Walker-Warburg syndrome, the most severe form of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...
    https://medlineplus.gov/genetics/gene/crppa - Genetics
  7. LARGE1 gene 
    ... the LARGE1 gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...
    https://medlineplus.gov/genetics/gene/large1 - Genetics
  8. POMT2 gene 
    ... the POMT2 gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes muscle weakness and abnormalities of the brain ...
    https://medlineplus.gov/genetics/gene/pomt2 - Genetics
  9. FKRP gene 
    ... the FKRP gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  10. Find a Neuromuscular Disease (Muscular Dystrophy Association)  
    Neuromuscular Disorders/Start Here ... Neuromuscular Disorders ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy ...
    https://www.mda.org/disease/list - External Health Links
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