Smith Mcginnis Syndrome Support

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Smith-Magenis syndrome - Genetics Home Reference - NIH

    https://ghr.nlm.nih.gov/condition/smith-magenis-syndrome
    Oct 29, 2019 · Smith-Magenis syndrome is a developmental disorder that affects many parts of the body. The major features of this condition include mild to moderate intellectual disability, delayed speech and language skills, distinctive facial features, sleep disturbances, and behavioral problems.

Smith-Magenis syndrome Genetic and Rare Diseases ...

    https://rarediseases.info.nih.gov/diseases/8197/smith-magenis-syndrome
    110 rows · Aug 28, 2017 · Smith-Magenis syndrome (SMS) is a developmental disorder that affects …

Smith-Magenis Syndrome Support - Facebook

    https://www.facebook.com/groups/149357361742618/
    Mission Statement and History PRISMS, an acronym for Parents and Researchers Interested In Smith-Magenis Syndrome, is dedicated to providing information and support to families of persons with...

PRISMS - Parents & Researchers Interested in Smith-Magenis ...

    https://www.prisms.org/
    I was interested in representing PRISMS and becoming a Regional Representative because I want to help families understand that even though the diagnosis of Smith Magenis Syndrome can be frightening and overwhelming, there is a strong community of support within PRISMS and from other families who experience this syndrome on a daily basis.

Smith-Magenis Syndrome - GeneReviews® - NCBI Bookshelf

    https://www.ncbi.nlm.nih.gov/books/n/gene/sms/
    Oct 22, 2001 · Smith-Magenis syndrome (SMS) is characterized by distinctive physical features (particularly facial features that progress with age), developmental delay, cognitive impairment, and behavioral abnormalities. Infants have feeding difficulties, failure to thrive, hypotonia, hyporeflexia, prolonged napping or need to be awakened for feeds, and generalized lethargy. The majority of …Cited by: 219

Smith-Magenis syndrome - Conditions - GTR - NCBI

    https://www.ncbi.nlm.nih.gov/gtr/conditions/C0795864/
    Smith-Magenis syndrome (SMS) is characterized by distinctive physical features (particularly facial features that progress with age), developmental delay, cognitive impairment, behavioral abnormalities, sleep disturbance, and childhood-onset abdominal obesity. Infants have feeding difficulties, failure to thrive, hypotonia, hyporeflexia, prolonged napping or need to be awakened for feeds, and ...

Smith-Magenis Syndrome (SMS) Foundation UK - Homepage

    https://smith-magenis.org/
    Supporting Families who have Children and Adults with Smith-Magenis Syndrome. The Smith-Magenis Syndrome Foundation is a small UK registered charity that supports families who have children of all ages with SMS and provides information for professionals working with these families.



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