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  1. Duchenne muscular dystrophy 
    https://medlineplus.gov/ency/article/000705.htm
    ... care provider if: Your child has symptoms of Duchenne muscular dystrophy Symptoms get worse, or new symptoms develop, particularly fever with cough or breathing problems
  2. Dystrophinopathies - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1119
    ... Constantin C, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010a; ...
  3. Part 2 – Children aged under 16 – signs and symptoms and investigative tests - Suspected neurological conditions - NCBI ... 
    https://www.ncbi.nlm.nih.gov/books/NBK542047
    ... laboratory’s upper limit of normal. An early diagnosis of Duchenne muscular dystrophy is important so that the family can undergo ... was aware that there is concern that the diagnosis of Duchenne muscular dystrophy (DMD) is delayed in some boys. The consensus ...
  4. 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 of HFI in ... M, Alagille D. Hereditary fructose intolerance in childhood. Diagnosis, management, and course ... dystrophy and hereditary fructose intolerance. Ital J Pediatr. 2012; ...
  5. Muscular Dystrophy 
    https://medlineplus.gov/musculardystrophy.html
    ... MD. Some of the more common types include: Duchenne muscular dystrophy, which is the most common childhood form. It is severe and affects boys more often than girls. The symptoms usually start between ages 3 and 6. Becker ...
  6. Rationale for categorising symptoms - Suspected neurological conditions - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK542058
    ... 18 months should be referred. The important differential diagnosis is Duchenne muscular dystrophy (DMD). A creatine kinase is a good screening test for Duchenne. The necessity to make this diagnosis early is to allow genetic counselling for family ...
  7. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... almost exclusively in males.</html:p><html:p >Duchenne and Becker muscular dystrophies have similar signs and symptoms and are caused by different mutations in the ...
  8. References - Suspected neurological conditions - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK542063
    ... JC, Banker BQ, Caskey CT, Golbus MS. Prenatal diagnosis of Duchenne’s muscular dystrophy. New England Journal of Medicine. 1977; 297(18): ...
  9. Guidelines - Noninvasive Positive Pressure Ventilation in the Home - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK554178
    ... 2011 72 Device initiation, monitoring, and candidate selection (Duchenne Muscular Dystrophy) KQ1 Carefully question and educate patients to report symptoms consistent with hypoventilation, including disturbed sleep, excessive daytime ...
  10. Data Abstraction Elements - Assessment and Management of Chronic Cough - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK116702
    ... etc.) Chronic bronchitis Bronchiectasis, Cystic Fibrosis Neuromuscular disease (Duchenne muscular dystrophy, ACS, SCI, etc.) Unexplained Other – Describe Positive signs/symptoms – Describe Positive diagnostic evaluation – Describe Other – Describe Specific ...
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