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  1. Facioscapulohumeral Muscular Dystrophy - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1443
    ... 9):564-72. Epub 2013 Aug 20. Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy in Patients Clinically Suspected of FSHD Using Optical Genome Mapping. [Neurol Genet. 2023] Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy in Patients Clinically Suspected of FSHD Using Optical ...
  2. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... in the upper arms (humeral). The signs and symptoms of facioscapulohumeral muscular dystrophy usually appear in adolescence. However, the onset and ... wheelchair.</html:p><html:p >Additional signs and symptoms of facioscapulohumeral muscular dystrophy can include mild high-tone hearing loss and ...
  3. Facioscapulohumeral muscular dystrophy 
    https://medlineplus.gov/ency/article/000707.htm
    Men often have more symptoms than women. Facioscapulohumeral muscular dystrophy mainly affects the face, shoulder, and upper arm muscles. However, it can also affect muscles around the pelvis, hips, and ...
  4. Muscular Dystrophy 
    https://medlineplus.gov/musculardystrophy.html
    ... age 2. They can be mild or severe. Facioscapulohumeral muscular dystrophy, which often ... the symptoms are How serious the symptoms are How quickly ...
  5. Muscular dystrophy 
    https://medlineplus.gov/ency/article/001190.htm
    ... dystrophy Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy Facioscapulohumeral muscular dystrophy Limb-girdle muscular dystrophy Oculopharyngeal muscular dystrophy Myotonic muscular dystrophy
  6. xmlmplus_topics_2025-03-12.xml 
    https://medlineplus.gov/xml/mplus_topics_2025-03-12.xml
    ... site ><information-category >Living ... and Tests</information-category><organization >Parent Project for ...
  7. Emery-Dreifuss Muscular Dystrophy - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1436
    ... Table 3. Disorders to Consider in the Differential Diagnosis of Emery-Dreifuss Muscular ... DNMT3B DUX4L1 SMCHD1 AD +++ (scapulo-peroneal) – – ...
  8. Calpainopathy - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1313
    ... A, López de Munain A. Dominant LGMD2A: alternative diagnosis or hidden digenism? Brain. ... muscular dystrophy and limb-girdle muscular dystrophy: "double trouble" overlapping ...
  9. Hereditary Myopathy with Early Respiratory Failure - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK185330
    ... Table 2. Disorders to Consider in the Differential Diagnosis of Hereditary Myopathy with Early ... dystrophy (FSHD) DNMT3B SMCHD1 3 AD Typically presents w/ ...
  10. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... topic><topic ><url >https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy</url><title >Facioscapulohumeral muscular dystrophy</title><other_names >< ...
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