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Results 1 - 10 of 29 for Larsen syndrome
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  1. Larsen syndrome 
    Larsen syndrome is a disorder that affects the development of bones throughout the body. The signs and symptoms of Larsen syndrome vary widely even within the same family. Affected ...
    https://medlineplus.gov/genetics/condition/larsen-syndrome - Genetics
  2. CHST3-related skeletal dysplasia 
    ... condition. It is sometimes known as autosomal recessive Larsen syndrome based on its similarity to another skeletal disorder called Larsen syndrome. Other names that have been used to describe ...
    https://medlineplus.gov/.../chst3-related-skeletal-dysplasia - Genetics
  3. FLNB gene 
    ... FLNB gene mutations have been identified that cause Larsen syndrome, a disorder that affects the development of bones ... and leading to the signs and symptoms of Larsen syndrome.It is not clear why similar mutations in ...
    https://medlineplus.gov/genetics/gene/flnb - Genetics
  4. Patient support and advocacy groups 
    ... Klippel-Trenaunay Support Group KS & A LAM Foundation Larsen Syndrome Resource Center Lesch-Nyhan Disease International Study Group ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  5. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
    https://medlineplus.gov/bonediseases.html - Health Topics
  6. CHST3 gene 
    ... caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis. Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/chst3 - Genetics
  7. Bernard-Soulier syndrome 
    ... Gudmundsdottir BR, Hilmarsdottir B, Vidarsson B, Magnusson MK, Larsen OH, Sorensen B, Ingerslev J, Onundarson PT. Clinical phenotype in heterozygote and biallelic Bernard-Soulier syndrome--a case control study. Am J Hematol. 2015 ...
    https://medlineplus.gov/genetics/condition/bernard-soulier-syndrome - Genetics
  8. Juvenile polyposis syndrome 
    ... Cerqueira D, Chinnathambi S, Pechman B, Bair J, Larsen-Haidle J, Howe JR. The ... of juvenile polyposis syndrome. J Gastroenterol Hepatol. 2005 Nov;20(11):1634- ...
    https://medlineplus.gov/.../condition/juvenile-polyposis-syndrome - Genetics
  9. What is Prader-Willi Syndrome? (Prader-Willi Syndrome Association)  
    Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by chronic hunger, growth hormone deficiency, and behavior challenges. ... Prader-Willi ...
    https://www.pwsausa.org/what-is-prader-willi-syndrome - External Health Links
  10. SMAD4 gene 
    ... update in 80 unrelated families with juvenile polyposis syndrome. J Med Genet. 2007 ... S, Pechman B, Bair J, Larsen-Haidle J, Howe JR. The rate of germline ...
    https://medlineplus.gov/genetics/gene/smad4 - Genetics
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