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Results 1 - 10 of 31 for crowded syndrome 1
  1. Hereditary hyperekplexia 
    ... this condition may have a low tolerance for crowded places and loud noises. People with ... The exact prevalence of hereditary hyperekplexia is ...
    https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia - Genetics
  2. Robinow syndrome 
    ... Smith syndrome Genetic Testing Registry: Autosomal dominant Robinow syndrome 1 Genetic Testing Registry: Autosomal recessive Robinow syndrome Genetic ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  3. Marfan syndrome 
    ... V, Vilacosta I, Bruna I, Fuster V. Marfan syndrome. Part 1: pathophysiology and diagnosis. Nat Rev Cardiol. 2010 May; ... Bartels R, Reinhardt DP. Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function. J ...
    https://medlineplus.gov/genetics/condition/marfan-syndrome - Genetics
  4. Apert syndrome 
    ... patches of missing hair in the eyebrows. Apert syndrome affects an estimated 1 in 65,000 to 88,000 newborns.Although ... Citation on PubMed Verma S, Draznin M. Apert syndrome. Dermatol Online J. 2005 Mar 1;11(1):15. No abstract available. Citation on ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  5. Helping Youth with CRPS Succeed in School (Reflex Sympathetic Dystrophy Syndrome Association of America) - PDF  
    Reflex Sympathetic Dystrophy Syndrome Association of America
    https://rsds.org/wp-content/uploads/2014/12/schoolbrochure_final.pdf - External Health Links
  6. What Is Marfan Syndrome? Easy-to-Read From the National Institutes of Health (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
    Marfan Syndrome is a disorder that affects connective tissue, which supports many parts of your body. Find out the symptoms, genetic causes & more. ... , Health Topic
    https://www.niams.nih.gov/health-topics/marfan-syndrome - External Health Links
  7. 48,XXYY syndrome 
    ... which affects communication and social interaction. 48,XXYY syndrome is estimated to affect 1 in 18,000 to 40,000 newborns who ... 24;1:42. doi: 10.1186/1750-1172-1-42. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
  8. Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDF  
    Ehlers-Danlos Syndrome/Learn More ... Ehlers-Danlos Syndrome ... Marfan Foundation ... PDF
    https://live-the-marfan-foundation-site.pantheonsite.io/...-Type.pdf - External Health Links
  9. MN1 C-terminal truncation syndrome 
    ... abnormalities, such as cone-shaped (conical ), jagged, or crowded teeth. Rarely, people with MCTT syndrome have premature fusion of certain skull bones (craniosynostosis). ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  10. Turner Syndrome: A Guide for Families (Turner Syndrome Society of the United States) - PDF  
    Turner Syndrome/Living With ... Turner Syndrome ... Turner Syndrome Society of the United States ... PDF
    https://media.wix.com/...8fb9de_3b42111faa254ab2b193ecb33f71e937.pdf - External Health Links
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