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Results 1 - 9 of 9 for "Walker-Warburg" syndrome
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  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. FKTN gene 
    ... gene mutations have been identified in people with Walker-Warburg syndrome, the most severe form of congenital muscular dystrophy. ... worldwide. Like Fukuyama congenital muscular dystrophy (described above), Walker-Warburg syndrome is associated with skeletal muscle weakness and eye ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  8. Birth Disorders of the Brain and Spinal Cord From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Craniofacial Abnormalities/Specifics ... Craniofacial ...
    https://www.ninds.nih.gov/.../birth-disorders-brain-and-spinal-cord - External Health Links
  9. 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