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316 results

  1. Becker muscular dystrophy 
    https://medlineplus.gov/ency/article/000706.htm
    Becker muscular dystrophy is very similar to Duchenne muscular dystrophy . The main difference is that it gets worse at a much slower rate and it is less common. This disease is caused by ...
  2. Fukuyama Congenital Muscular Dystrophy - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1206
    ... muscle degeneration and regeneration, which distinguishes FCMD from Duchenne muscular dystrophy . Immunohistochemical staining using alpha-dystroglycan antibody reveals selective ...
  3. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... onset, and rate of progression. In boys with Duchenne muscular dystrophy, muscle weakness tends to appear in early childhood ... become life-threatening in most cases. Males with Duchenne muscular dystrophy typically live into their twenties, while males with ...
  4. Barth Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK247162
    ... LVNC and skeletal myopathy can be seen in Duchenne muscular dystrophy , with a prevalence as high as 28% [ Statile et al 2013 ]. However, in Duchenne muscular dystrophy (in contrast to Barth syndrome) the LVNC tends ...
  5. pdfNLM Technical Bulletin, no.249-257 
    https://www.nlm.nih.gov/.../nlmarchives/techbull/249-257-1990.pdf
    ... CHROMOSOMAL DISORDERS DOWN'SSYNDROME XYY KARYOTYPE CYSTIC FIBROSIS DUCHENNE MUSCULAR DYSTROPHY HEMOPHILIA HUNTINGTON'S CHOREA PHENYLKETONURIA SICKLE CELL ANEMIA TAY ...
  6. xmlmplus_topics_2025-08-09.xml 
    https://medlineplus.gov/xml/mplus_topics_2025-08-09.xml
    ... the more common types include:</p> <ul> <li>Duchenne muscular dystrophy, which is the most common childhood form. It ... Neurological Disorders and Stroke</primary-institute><see-reference >Duchenne ... ><information-category >Genetics</information-category>< ...
  7. Disabilities 
    https://medlineplus.gov/disabilities.html
    ... can include: Disorders in single genes, such as Duchenne muscular dystrophy Disorders of chromosomes, such as Down syndrome Exposures ( ...
  8. Guideline summary - Suspected neurological conditions - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK542064
    ... boy, consider measuring creatinine kinase level to exclude Duchenne muscular dystrophy before the boy has had a specialist review. ... boy, consider measuring creatine kinase level to exclude Duchenne muscular dystrophy before the boy has had a specialist review. ...
  9. Excluded Studies - Cerebral palsy in under 25s: assessment and management - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK533212
    ... G., Update on neuromuscular disorders in pediatric orthopaedics: Duchenne muscular dystrophy, myelomeningocele, and cerebral palsy, Journal of Pediatric Orthopaedics, ...
  10. Hereditary Fructose Intolerance - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK333439
    ... other conditions (e.g., phenylketonuria , celiac disease , and Duchenne muscular dystrophy ) has delayed diagnosis and/or initiation of treatment ... and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance. Ital J Pediatr. 2012; ...
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