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Results 11 - 19 of 19 for Duchenne muscular dystrophy
  1. Disabilities (National Library of Medicine)  
    ... can include: Disorders in single genes, such as Duchenne muscular dystrophy Disorders of chromosomes, such as Down syndrome Exposures ( ...
    https://medlineplus.gov/disabilities.html - Health Topics
  2. Muscle biopsy 
    ... and a skin rash ( dermatomyositis ) Various muscular dystrophies ( Duchenne muscular dystrophy and other conditions) Destruction of the muscle ( myopathic ...
    https://medlineplus.gov/ency/article/003924.htm - Medical Encyclopedia
  3. X-linked dilated cardiomyopathy 
    ... cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 1993 ...
    https://medlineplus.gov/.../x-linked-dilated-cardiomyopathy - Genetics
  4. Genetic Testing (For Parents) Video (Nemours Foundation)  
    ... spina bifida Turner syndrome von Willebrand Disease albinism Duchenne muscular dystrophy In some cases, it also can show how ...
    https://kidshealth.org/en/parents/genetics.html - Videos
  5. Genetics 
    ... Phenylketonuria (PKU) Sickle cell anemia X-linked recessive: Duchenne muscular dystrophy Hemophilia A Autosomal dominant: Familial hypercholesterolemia Marfan syndrome ...
    https://medlineplus.gov/ency/article/002048.htm - Medical Encyclopedia
  6. Sex-linked recessive 
    ... protect the male. Diseases such as hemophilia and Duchenne muscular dystrophy occur from a recessive gene on the X ...
    https://medlineplus.gov/ency/article/002051.htm - Medical Encyclopedia
  7. Electromyography 
    ... problem affecting the median nerve in the arm) Duchenne muscular dystrophy (inherited disease that involves muscle weakness) Facioscapulohumeral muscular ...
    https://medlineplus.gov/ency/article/003929.htm - Medical Encyclopedia
  8. NR0B1 gene 
    ... the deletion also includes the gene associated with Duchenne and Becker muscular dystrophy. People with this larger deletion have progressive muscle ...
    https://medlineplus.gov/genetics/gene/nr0b1 - Genetics
  9. X-linked adrenal hypoplasia congenita 
    ... with hypoplasia congenita and other diseases, such as Duchenne and Becker muscular dystrophy and glycerol kinase deficiency. NR0B1 This condition is ...
    https://medlineplus.gov/.../x-linked-adrenal-hypoplasia-congenita - Genetics
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