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Results 1 - 10 of 338 for Congenital muscular dystrophy
  1. Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
  2. LMNA-related congenital muscular dystrophy (L-CMD) is a condition that primarily affects muscles used for movement (skeletal muscles). It is part of a group ...
  3. ... spine muscular dystrophy (RSMD) is a form of congenital muscular dystrophy. Disorders in this group cause muscle weakness and ... not show signs and symptoms of the condition. Congenital muscular dystrophy with spine rigidity syndrome Muscular dystrophy, congenital, merosin- ...
  4. ... intermediate form is moderate in severity, and Ullrich congenital muscular dystrophy is the most severe.People with Bethlem muscular ... mechanical ventilation), particularly during sleep.People with Ullrich congenital muscular dystrophy have severe muscle weakness beginning soon after birth. ...
  5. ... FKTN gene have been found to cause Fukuyama congenital muscular dystrophy, a condition that causes skeletal muscle weakness and brain and eye abnormalities. This form of congenital muscular dystrophy is seen almost exclusively in Japan. Virtually everyone ...
  6. ... of a group of genetic conditions known as congenital muscular dystrophies, which cause muscle weakness and wasting (atrophy) beginning ... brain and eye anomalies], type A Walker-Warburg congenital muscular dystrophy Genetic Testing Registry: Walker-Warburg congenital muscular dystrophy ...
  7. ... symptoms of the condition. EOMFC Salih CMD Salih congenital muscular dystrophy Salih myopathy Titinopathy & early-onset myopathy with fatal ... A, Campbell KP. A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics. 1998 Dec;29(6): ...
  8. ... VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
  9. ... VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
  10. ... VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
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