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Results 1 - 10 of 13 for Congenital muscular dystrophy
  1. Fukuyama congenital muscular dystrophy 
    Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  2. LMNA-related congenital muscular dystrophy 
    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 ...
    https://medlineplus.gov/...mna-related-congenital-muscular-dystrophy - Genetics
  3. Rigid spine muscular dystrophy 
    ... 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- ...
    https://medlineplus.gov/.../condition/rigid-spine-muscular-dystrophy - Genetics
  4. Collagen VI-related dystrophy 
    ... 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. ...
    https://medlineplus.gov/.../condition/collagen-vi-related-myopathy - Genetics
  5. Walker-Warburg syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  6. Early-onset myopathy with fatal cardiomyopathy 
    ... 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): ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  7. LAMA2-related muscular dystrophy 
    ... part of a class of muscle disorders called congenital muscular dystrophies and is sometimes called congenital muscular dystrophy type 1A. Affected infants may have severe muscle ...
    https://medlineplus.gov/.../lama2-related-muscular-dystrophy - Genetics
  8. Myotonic dystrophy 
    ... part of a group of inherited disorders called muscular dystrophies. It is the most common form of muscular dystrophy that begins in adulthood.Myotonic dystrophy is characterized ...
    https://medlineplus.gov/genetics/condition/myotonic-dystrophy - Genetics
  9. Multiminicore disease 
    ... N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing ... Sewry C, Phadke R, Gautel M, Muntoni F. Congenital myopathies: disorders of excitation-contraction coupling and muscle ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  10. X-linked adrenal hypoplasia congenita 
    ... and other diseases, such as Duchenne and Becker muscular dystrophy and glycerol kinase deficiency. NR0B1 This condition is ... hypoplasia congenita X-linked AHC Genetic Testing Registry: Congenital adrenal hypoplasia, X-linked X-linked adrenal hypoplasia ...
    https://medlineplus.gov/.../x-linked-adrenal-hypoplasia-congenita - Genetics
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