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Results 1 - 8 of 8 for "Smith-Magenis"
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  1. Smith-Magenis syndrome 
    Smith-Magenis syndrome is a developmental disorder that affects behavior, emotions, and learning processes. The major features of this condition include distinctive ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  2. RAI1 gene 
    ... megabases (Mb). (A deletion of this segment causes Smith-Magenis syndrome, described below.) In the remaining one-third ... for most of the signs and symptoms of Smith-Magenis syndrome. The major features of this condition include ...
    https://medlineplus.gov/genetics/gene/rai1 - Genetics
  3. Tasimelteon 
    ... children 3 years of age and older with Smith-Magenis Syndrome (SMS; a developmental disorder). Tasimelteon is in ...
    https://medlineplus.gov/druginfo/meds/a615004.html - Drugs and Supplements
  4. Chromosome 17 
    ... Potocki-Lupski syndrome. More About This Health Condition Smith-Magenis syndrome usually results from a deletion of a ... p arm designated p11.2. The features of Smith-Magenis syndrome include mild to moderate intellectual disabilities, delayed ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  5. Potocki-Lupski syndrome 
    ... of this segment causes a related condition called Smith-Magenis syndrome.) In the remaining one-third of cases, ... L. Neurodevelopmental Disorders Associated with Abnormal Gene Dosage: Smith-Magenis and Potocki-Lupski Syndromes. J Pediatr Genet. 2015 ...
    https://medlineplus.gov/genetics/condition/potocki-lupski-syndrome - Genetics
  6. Developmental Disabilities (National Library of Medicine)  
    What are developmental disabilities? Developmental disabilities are conditions that are usually present at birth. They can affect a child's growth and ...
    https://medlineplus.gov/developmentaldisabilities.html - Health Topics
  7. Patient support and advocacy groups 
    ... Project Muscular Dystrophy Parents and Researchers Interested in Smith-Magenis Syndrome PCD Family Support Group PCOS Awareness Association ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  8. MBD5-associated neurodevelopmental disorder 
    ... sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes. Eur J Hum Genet. ...
    https://medlineplus.gov/...d5-associated-neurodevelopmental-disorder - Genetics