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Results 1 - 7 of 7 for "Walker-Warburg" congenital muscular dystrophy
Did you mean "Walker-marburg" congenital muscular dystrophy?
  1. Walker-Warburg syndrome 
    ... dystroglycanopathy [with brain and eye anomalies], type A Walker-Warburg congenital muscular dystrophy Genetic Testing Registry: Walker-Warburg congenital muscular dystrophy ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. FKTN gene 
    ... condition is found in populations worldwide. Like Fukuyama congenital muscular dystrophy (described above), Walker-Warburg syndrome is associated with skeletal muscle weakness and ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics