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Results 1 - 6 of 6 for "Walker-Warburg" congenital muscular dystrophy
Did you mean "Walker-marburg" congenital muscular dystrophy?
  1. POMT2 gene 
    ... form of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes muscle weakness and abnormalities of the brain ... past early childhood.POMT2 gene mutations that cause Walker-Warburg syndrome lead to the formation of nonfunctional POMT enzyme ...
    https://medlineplus.gov/genetics/gene/pomt2 - Genetics
  2. LARGE1 gene 
    ... 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/large1 - Genetics
  3. FKRP gene 
    ... 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/fkrp - Genetics
  4. CRPPA gene 
    ... 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
  5. POMT1 gene 
    ... form of a group of disorders known as congenital muscular dystrophies. Individuals with Walker-Warburg syndrome have skeletal muscle weakness and abnormalities of ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
  6. FKTN gene 
    ... severe than those seen in people with Fukuyama congenital muscular dystrophy. Children with Walker-Warburg syndrome tend to survive only into infancy or ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics