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- 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 ...
- The FKTN gene (formerly known as FCMD) provides instructions for making a protein called fukutin. This protein is present in many of the body's tissues but is particularly ...
- ... symptoms of the condition. Cerebromuscular dystrophy, Fukuyama type FCMD Fukuyama CMD Fukuyama muscular dystrophy Fukuyama syndrome Fukuyama ... T, Matsumura K. Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy. Congenit Anom (Kyoto). 2003 Jun; ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...