Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Search help
237 results
  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. NLM Digital Collections - Genetic counseling on the hereditary neuromuscular diseases 
    Publication: [Bethesda, Md.] : The Institute ; [Atlanta : for loan by National Medical Audiovisual Center ; Washington : for sale by National Audiovisual Center], 1976
    resource.nlm.nih.gov/7801638A
    ... cultured amniotic cells. Ah In the cases of Duchenne muscular dystrophy, ah prenatal diagnosis is less successful. However, if the fetus of ... proven to be defective. In the case of Duchenne muscular dystrophy. However, the diagnosis of a male fetus does not determine whether ...
  7. 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 ...
  8. NLM Digital Collections - Valor da semeiologia ocular da molestia de Duchenne e sua importancia diagnostica no estadio .... 
    Publication: Bahia : Typ. do Salvador-Cathedral, 1908
    resource.nlm.nih.gov/101722020
    Muscular Dystrophy, Duchenne -- diagnosis ... doutor em medicina Bittencourt, Luiz de Lima, author. Muscular Dystrophy, Duchenne -- diagnosis Early Diagnosis Eye Manifestations Bahia : Typ. do Salvador- ...
  9. 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 ...
  10. 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): ...
first · previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next · last