81. AllRefer Health - Marfan Syndrome marfan syndrome information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests, support groups, http://health.allrefer.com/health/marfan-syndrome-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Marfan Syndrome Marfan Syndrome Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Definition Marfan syndrome is an inheritable disorder of connective tissue (which adds strength to the body's structures) that affects the skeletal system, cardiovascular system, eyes, and skin. Pectus Excavatum Marfan's Syndrome Marfan syndrome is inherited as an autosomal dominant trait. However, up to 30% of cases have no family history and are so called "sporadic" cases. In sporadic cases, Marfan syndrome is believed to result from a spontaneous new mutation. Marfan syndrome is caused by mutations in the gene fibrillin-1. Fibrillin-1 plays an important role as the scaffolding for elastic tissue in the body. Disruption of such scaffolding (by mutations in fibrillin-1) thus results in changes in elastic tissues, particularly in the aorta, eye, and skin. Mutations in fibrillin-1 also cause overgrowth of the long bones of the body, resulting in the tall stature and long limbs seen in Marfan patients.

82. MoSt GeNe/Genetic Drift/Management Of Common Genetic Disorders marfan syndrome is an autosomal dominant, highly penetrant, About 15% of individuals with marfan syndrome have new mutations; the rest are familial. http://www.mostgene.org/gd/gdvol16e.htm

Previous Section This Issue- Table of Contents Next Section Management of Common Genetic Disorders Vol. 16: Summer, 1998 Marfan Syndrome Introduction Marfan syndrome is an autosomal dominant, highly penetrant, disorder of connective tissue with extremely variable clinical expression. The frequency is 1 to 10 per 100,000 live births. About 15% of individuals with Marfan syndrome have new mutations; the rest are familial. It is caused by a defect in the fibrillin-1 gene (FBN1) on chromosome 15. Many different mutations of FBN1 have been identified, which may contribute to the variability seen in the disorder. Currently, no single gene probe or group of probes can detect most FBN1 mutations. Sequencing the entire gene for mutations is tedious, and often detects mutations that may represent normal variation, resulting in both false positives and false negatives. Immunohistological evaluation of skin for abnormal fibrillin has been reported but is not widely available. For now, diagnosis of Marfan syndrome remains a clinical one. Clinical Features Marfan syndrome typically affects three major body systems: cardiovascular, skeletal, and ocular. Lungs and/or skin may also be involved.

83. Treatment Of Marfan Syndrome, Mayo Clinic In Rochester, Minn. marfan syndrome at Mayo Clinic in Rochester. marfan syndrome is a disorder of the connective tissue in the body. It can affect the skeletal system, http://www.mayoclinic.org/marfan-rst/

Home About Mayo Clinic Jobs Contact Us Mayo Clinic Locations: Arizona Florida Minnesota Mayo Clinic ... Medical Services Marfan Syndrome Marfan Syndrome Treatment Features and Diagnosis Heart Surgery Frequent Questions ... Medical Services Treatment of Marfan Syndrome at Mayo Clinic in Rochester Successful heart surgery at Mayo Clinic allows Heather Hinton to live a normal life despite rare genetic disorder. Read Heather's story. Marfan syndrome is a disorder of the connective tissue in the body. It can affect the skeletal system, blood vessels, heart, lungs, eyes and other organ systems. Marfan syndrome can be inherited from either parent, or it can result from a new change in genetic material. There is a 50-50 chance that children will inherit the disorder from their parent. Approximately 200,000 people in the United States have Marfan syndrome, and it can occur in men or women of any race or ethnic group. Many affected individuals are young adults, adolescents or children. Marfan Syndrome Clinic Mayo Clinic offers an integrated genetic, medical and surgical team of Mayo physicians in the Marfan Clinic to provide diagnosis and treatment for patients with Marfan syndrome. The Marfan Clinic allows patients to access a variety of specialty physicians cardiologists (heart)

84. Treatment Of Marfan Syndrome, Mayo Clinic In Jacksonville, Fla. Treatment of marfan syndrome at Mayo Clinic Jacksonville. http://www.mayoclinic.org/marfan-jax/

Home About Mayo Clinic Jobs Contact Us Mayo Clinic Locations: Arizona Florida Minnesota Mayo Clinic ... Medical Services Marfan Syndrome Marfan Syndrome Treatment Features and Diagnosis Heart Surgery Appointments ... Medical Services Treatment of Marfan Syndrome at Mayo Clinic in Jacksonville Marfan syndrome is a disorder of the connective tissue in the body. It can affect the skeletal system, blood vessels, heart, lungs, eyes and other organ systems. Marfan syndrome can be inherited from either parent, or it can result from a new change in genetic material. There is a 50-50 chance that children will inherit the disorder from their parent. About 200,000 people in the United States have Marfan syndrome. It can occur in men or women of any race or ethnic group. Many affected individuals are young adults, adolescents or children. Treatment of Marfan syndrome depends on the patient's affected organ systems. Currently, a cure does not exist, but medical care can improve prognosis and life span. Patients at Mayo Clinic work closely with their team of specialists to create a treatment plan. Genetic and reproductive counseling is an important part of caring for patients and families with Marfan syndrome.

85. Discovery Health :: Diseases & Conditions :: Marfan Syndrome marfan syndrome is an inherited disorder of the connective tissue in the body. It affects mainly the muscles, bones, eyes, and heart. http://health.discovery.com/encyclopedias/illnesses.html?article=3401&page=1

86. Barnes-Jewish Hospital - Marfan Syndrome Center marfan syndrome is a genetic disorder of the connective tissue that affects many organ Some experts suspect Abe Lincoln may have had marfan syndrome. http://www.barnesjewish.org/groups/default.asp?NavID=895

87. Marfan Syndrome, Cincinnati Children's Hospital Medical Center marfan syndrome manifestations, causes, diagnosis, treatment, and prognosis information from the Heart Encyclopedia by Cincinnati Children s Hospital http://www.cincinnatichildrens.org/health/heart-encyclopedia/disease/syndrome/ma

Home Contact Us Site Map Go to Advanced Search ... Down Syndrome Marfan Syndrome Velo-Cardio-Facial Syndrome VACTERL or VATER Association Signs and Symptoms Cardiac-Related Diagnostic Methods ... Contact Us Heart-Related Syndromes Marfan Syndrome Manifestations, Causes, Diagnosis, Treatment, Prognosis Explanation Manifestations Causes Diagnosis ... Prognosis What is Marfan syndrome? The Marfan syndrome is a genetic disorder that affects the body's connective tissues, or the tissues in between the main cells of each organ of the body. All organs contain connective tissue and, hence, the manifestations of Marfan syndrome appear in many parts of the body, especially the skeletal system, the eyes, the heart and blood vessels and the lungs. The term "syndrome" refers to the collection of physical findings that occur together often enough to provide a recognizable pattern that allows the diagnosis to be made. It was first described in a six year old girl by the French pediatrician, Antoine Marfan, in 1896. Return to Top Manifestations of Marfan syndrome The heart is affected in nearly 80 percent of patients with this syndrome. The most important finding is enlargement or dilation of the aorta, the main blood vessel that carries blood to the body. This abnormality in connective tissue of the first few inches of the aorta allows the aorta to stretch sufficiently to cause tearing or rupture.

88. Division Of Medical Genetics - Marfan Syndrome Clinical Services of the Division of Medical Genetics, Department of Medicine, University of Pennsylvania Health System. http://www.uphs.upenn.edu/penngen/clinical/marfan.html

Home Clinical Services Cancer Genetics Hemochromatosis HHT Center Marfan Syndrome Metabolism Neurofibromatosis Tuberous Sclerosis VHL Center Research Education Faculty/Staff ... Contact Us Division of Medical Genetics Marfan Syndrome and Related Connective Tissue Disorders Center Reed E. Pyeritz, M.D., Ph.D., Director This center is dedicated to the comprehensive evaluation and management of children and adults with a known or suspected diagnoses of Marfan syndrome or related conditions such as MASS phenotype, familial ectopia lentis (dislocated lenses), or familial aortic aneurysm. We provide coordinated multidisciplinary care including diagnosis, genetic testing, education, genetic counseling, management and support. Physicians participating in this center include specialists in: Cardiology Cardiovascular surgery Medical Genetics Obstetrics and gynecology Ophthalmology Orthopedics Radiology All of these physicians have special experience in treating patients with Marfan syndrome and related disorders. Visits to the Center are coordinated by the Division of Medical Genetics. Appointments can be made by calling Olga Slotiuk, the Clinic Coordinator at 215-662-4740 or through e-mail at: medgenclinic@uphs.upenn.edu

89. BBC - Health - Conditions - Marfan Syndrome A guide to marfan syndrome. marfan syndrome is an inherited disorder of the connective tissues. There s no cure, but careful medical and surgical http://www.bbc.co.uk/health/conditions/marfan1.shtml

@import url('/includes/tbenh.css') ; Home TV Radio Talk ... A-Z Index FRIDAY 9th September 2005 Text only BBC Homepage Lifestyle Health ... Help Like this page? Send it to a friend! Marfan syndrome Dr Trisha Macnair Marfan syndrome is an inherited disorder of the connective tissues. There's no cure, but careful medical and surgical management, and lifestyle changes, can greatly improve the prognosis and lengthen life span. In this article How does the disease develop? Who is affected? Further help How does the disease develop? The abnormal gene usually controls production of a protein called fibrillin. Fibrillin plays an important part in the normal structure or 'scaffolding' of connective tissue throughout the body. When abnormal protein is produced, the structure of the connective tissue is abnormal and weak. Severity varies, but on average one in ten is seriously affected. It affects many organs including the skeleton, lungs, eyes, heart and blood vessels. Those with the condition are usually characteristically tall and slim with long fingers and loose joints. Who is affected?

90. Big's Place - Marfan Syndrome marfan syndrome os a genetic disorder of the connective tissue that can affect marfan syndrome National Marfan Foundation Canadian Marfan Association http://www.bigsplace.com/marfan.html

Marfan Syndrome These links are provided as a resource for anyone interested in finding information on Marfan Syndrome. Marfan Syndrome os a genetic disorder of the connective tissue that can affect the skelatal system, eyes, lungs, blood vessels and heart. By Category or Subject Marfan Syndrome Articles/Research Marfan Syndrome National Marfan Foundation Canadian Marfan Association UK Marfan Association Marfan Hilfe (Deutschland) ... A Diary about Marfans Articles/Research Marfan Syndrome - H.Oberman Marfan Syndrome - F. Matsen, M.D. Should you have a link related to Marfan Syndrome that you feel is absent from this page, please e-mail it to: admin@bigsplace.com E-Mail us! Last Updated: October 26, 2003 Go to... Home Asperger's Syndrome ADD/ADHD Page 1 ADD/ADHD Page 2 Autism Spectrum Bipolar Disorder Manic Depression Marfan Syndrome Medications Oppositional Defiance Panic Disorder Sensory Integration Message Boards Awards Advertising Policy

91. MARFAN SYNDROME: JR FACT SHEET Living with marfan syndrome is what this site is all about. The life story of Jon, and how he has learned to cope over the years. http://www.jrmarfan58.com/

MARFAN SYNDROME: JR FACT SHEET Living with Marfans E-Mail ... JRMarfan58@aol.com ..... My name is Jon. I am a 46 year old Boston man who lives with a condition known as MARFAN SYNDROME. IMPORTANT PLEASE NOTE: This website is an outline of my life and research that I have done over the last 5 years. It in no way represents all Marfan cases. Information contained in this website is intended for informational purposes only. It is not intended to be a substitute for medical advice. See your physician with any and all questions regarding your medical condition. MARFAN SYNDROME: - A HARD LOOK - (Excerpts from the National Marfan Foundation) MARFAN SYNDROME is a progressive, incurable, genetic disorder of the connective tissue, frequently characterized by tall stature, long limbs and fingers, scoliosis, cardial complications and subluxatin of the lenses of the eyes. The greatest threat to life is from the cardiovascular deterioration which causes aneurysms. The associated orthopedic and opthalmological problems can cause severe handicapping including loss of mobility, chronic and debilitating pain and blindness. Medical reporting lags behind the reality of the severe manifestations of the Marfan Syndrome. It is only in the last few years that attention has been directed to this disorder. At this time there in no therapy or treatment to lessen deteriorating muscular and skeletal degeneration. Links 2 Related Conditions Pictures SS Disabilty Checklist ... Aortic Aneurysms-Facts

92. Marfan Syndrome -- From WebMD Learn about marfan syndrome from WebMD and the doctors at The Cleveland Clinic. http://my.webmd.com/content/pages/14/81967

WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in All Conditions ADD/ADHD Allergies Alzheimer's Arthritis Asthma Back Pain Bipolar Disorder Breast Cancer Cancer Cholesterol Management Dental Depression Diabetes Epilepsy Eye Health Heart Disease Hepatitis HIV/AIDS Hypertension Men's Conditions Mental Health Migraines/Headaches Multiple Sclerosis Osteoporosis Parkinson's Sexual Conditions Stroke Weight Control Women's Conditions WebMD Medical Reference in collaboration with Get the Facts Coronary Heart Disease Risk Factors Abnormal Heart Rhythms ... Other Heart Problems Other Diseases Vascular Diseases Carotid Artery Disease Stroke Aortic Aneurysm ... To the Heart Center Heart Disease: Marfan Syndrome Marfan syndrome is an inherited disease that affects the connective tissue. Connective tissue is the most abundant tissue in the body and is a vital component to supporting the body's organs. Its primary purpose is to hold the body together and provide a framework for growth and development. It provides the strength and support to tendons, cartilage, heart valves and many other parts of the body, as well as strength and elasticity to the blood vessels. For people with Marfan syndrome, the chemical makeup of the connective tissue isn't normal and as a result is not as strong as it should be.

93. Marfan Syndrome marfan syndrome Updated April 4, 2004 marfan syndrome Your Genes, Your Health Flash application; marfan syndrome American Heart Association http://www.noah-health.org/en/genetic/conditions/marfan/

Skip navigation About NOAH Help English Spanish Both Advanced NOAH Genetic Diseases Change text size: Marfan Syndrome Updated: April 4, 2004 The Basics Heart Conditions: Marfan Syndrome Canadian Heart Foundation (also in French Marfan Syndrome: Genes and Disease National Center for Biotechnology Information Marfan Syndrome Fact Sheet Canadian Marfan Association Marfan Syndrome Resource Manual National Marfan Foundation Marfan Syndrome March of Dimes (NOAH Provider) (also in Spanish Marfan Syndrome Your Genes, Your Health Marfan Syndrome American Heart Association The Marfan Syndrome University of Washington Fact Sheet National Marfan Foundation Questions and Answers About Marfan Syndrome National Institute of Arthritis and Musculoskeletal Diseases (also in Spanish Information Resources National Marfan Foundation National Marfan Foundation Connecticut Chapters National Marfan Foundation New Jersey Chapters National Marfan Foundation New York Chapters Researched by NOAH Contributing Editor: NOAH Team NOAH Genetic Diseases Specific Conditions > Marfan Syndrome Health Topics Index A to Z Page of the Month Advanced Search ... Feedback

94. Marfan's Syndrome ICD9-CM 759.82 marfan syndrome REFERENCES; Cistulli PA, et al. Replacement of the aortic root in patients with Marfan s syndrome. http://www.5mcc.com/Assets/SUMMARY/TP0565.html

Marfan's syndrome DESCRIPTION: A dominantly inherited disorder of connective tissue (elastic fibers) affecting primarily the musculoskeletal system, the cardiovascular system and the eye System(s) affected: Musculoskeletal, Endocrine/Metabolic Genetics: Autosomal dominant with high penetrance; 15% spontaneous mutation Incidence/Prevalence in USA: 1 in 10,000 - 20,000 (estimated 1 in 15,000) Predominant age: Congenital, so disorder is present from birth. However clinical manifestations do not usually become apparent until adolescence or young adulthood. Predominant sex: No gender, ethnic or racial predilection CAUSES: Genetic; at least 5% are obviously familial, the remainder arise from apparent spontaneous mutations ICD-9-CM: 759.82 Marfan syndrome REFERENCES: Cistulli PA, et al. Relationship between craniofacial abnormalities and sleep disturbed breathing in Marfan’s syndrome. Chest 2001;120(5):1455-60 Carley ME, et al. Urinary incontinence and pelvic organ prolapse in women with Marfan's syndrome. Am J Obstet Gynecol 2000;182(5):1021-3 Gott VL, et al. Replacement of the aortic root in patients with Marfan's syndrome. New Engl J Med 1999;340(17):1307-13

95. Heart And Stroke Foundation Of Canada marfan syndrome is a connective tissue disorder. Connective tissue provides substance and support to tendons, ligaments, blood vessels, cartilage, http://ww2.heartandstroke.ca/Page.asp?PageID=33&ArticleID=567&Src=heart&From=Sub

96. Salon.com People | Does Bin Laden Have Marfan Syndrome? marfan syndrome is a potentially fatal disorder of connective tissue, Although marfan syndrome, like sickle cell anemia, is often the product of an http://www.salon.com/people/feature/2001/11/09/marfan/

Search About Salon Table Talk Advertise in Salon ... Search All of Salon.com Only People Directory Hot Topics Amy Reiter's Nothing Personal Cheek Catherine Keener Rudy Giuliani ... Steve Earle Articles by date All of Salon.com By department The Movie Page Books ... Table Talk [Spirited Salon forums] Mother, May I Drink from the Funnel? Concept your own Lifetime TV movie. There's no place like home Savoring the end of "Oz." Posts of the week The Well [Pioneering members-only discussions] What do Miles Davis and hurricanes have in common? Sound Off E-mail Salon Send us a Letter to the Editor Today's letters Downloads Get Salon.com on your PDA Does bin Laden have Marfan Syndrome? Is Osama suffering from a rare disease that can cause sudden death? By Mark Francis Cohen If what some medical experts say is true, it may not require a military strike to kill Osama bin Laden. For several years now, reports have been circulating that claim the 45-year-old is quite ill, sees doctors regularly and may have a heart problem. The evidence is sketchy, but some see signs that bin Laden could die suddenly. Marfan syndrome is a potentially fatal disorder of connective tissue, and some believe it's jeopardizing the life of al-Qaida's elusive leader. Bin Laden would be in good company: Some say Marfan would have killed Abraham Lincoln if John Wilkes Booth had missed his mark in 1865. It also appears to have claimed the lives of Jonathan Larson, author of the musical "Rent," who died on the eve of the production's 1996 Broadway debut; Chris Patton, a University of Maryland basketball star who died during a pickup game; and Flo Hyman, an Olympic volleyball player who died at 31 in 1986. The aortas of all three ripped in a manner consistent with the disorder. Charles de Gaulle and composer Sergei Rachmaninoff are also believed to have had Marfan.

97. Welcome To Marfan Support And Information In NSW Australia Homepage of Marfan Support and Information, NSW Australia. about marfan syndrome about this website aorta dissection archives 2004 http://www.marfan.net.au/

Marfan Support and Information in NSW home about marfan syndrome about this website aorta dissection ... resources Welcome to Marfan support and information in NSW ! left - Jaxon ; middle and right - Richard, my son. - This website is a personal website, see page about this website * To download a pdf.file you'll need Adobe Reader , which you can install here Noticeboard September 2005 See the Marfan symposium in Ghent Program for September 14-17 Marfan documentary Jabe Babe, a heightened life, will be broadcast by SBS on 15nov05 at 10pm. See index page Jabe Babe In Travelling Australia our trip on the Ghan from South to North. The page Internet and other news frequently as 'new' additions. Green words or names means link connections - press on them

98. Job Accommodation Network marfan syndrome is a genetic disorder of the connective tissue that can affect the skeleton, Accommodation ideas for individuals with marfan syndrome http://www.jan.wvu.edu/soar/other/marfan.html

Job Accommodation Network's Searchable Online Accommodation Resource (SOAR) Accommodation Ideas Marfan Syndrome Marfan syndrome is a genetic disorder of the connective tissue that can affect the skeleton, lungs, eyes, heart, and blood vessels. The condition affects both men and women of any race or ethnic group. It is estimated that at least 200,000 people in the United States have Marfan syndrome or a related connective tissue disorder. Characteristics of the disorder vary greatly, but the most common problems associated with Marfan syndrome include heart problems, scoliosis, and near-sightedness. There is no cure for the disorder yet, but careful medical management can greatly improve the prognosis and lengthen the life span. Accommodation ideas for individuals with Marfan syndrome: Fatigue: Fatigue is often associated with Marfan syndrome. Possible solutions include a reduced work schedule, periodic rest breaks, a transfer to a less physically demanding job, and the flexible use of leave time. Individuals may also benefit from implementing ergonomic principles. For additional information on ergonomics, visit: Ergonomics in the Workplace: A Resource Guide Lifting Materials, Products, and People:

99. Webhealth | Health Information On The Web marfan syndrome is a variable condition of the connective tissue of the from marfan syndrome. Information Courtesy of The Marfan Association http://www.webhealth.co.uk/a_to_z_of_health/marfan_syndrome.asp

Free Radicals Test A - Z of Health Research Therapy Overviews ... Support Groups Members Area Update your details Lost password Discussion groups Practitioner Search ... Join Our Directories MARFAN SYNDROME Marfan syndrome is a variable condition of the connective tissue of the body and may affect the eyes, skeleton, lungs, heart and blood vessels. It is hereditary in 75% of cases and spontaneous in 25%. There is a 50/50 chance of passing on the marfan gene to each child from an affected parent. A classic Marfan sufferer is usually tall and thin with long arms and legs, the joints of which are often lax and painful and prone to dislocation. Diagnosis is sometimes first made by an optician as the lens can dislocate ( which happens in few other conditions ) and retinal detachment may also occur. The skeleton is often affected by scoliosis and this twisting of the spine can cause chest deformity. ( Pigeon chest or dipped - chest )

100. Tokyo Medical University Genetics Marfan Syndrome marfan syndrome(22K). Aortic root dilatation, Aortic regurgitation ( ), Mitral regurgitation and Mitral valve prolapse ( ). aneurysms(7K) http://www.tokyo-med.ac.jp/genet/ms/mrf-e.htm

Tokyo Medical University Department of Paediatircs Genetics Study Group Hironao NUMABE, M.D. E-mail: hnumabe@tokyo-med.ac.jp Japanese Page is Here. Marfan Syndrome Images: Autosomal dominant fibrillin-1(FBN1) gene mutation normal(23K) : Tricuspid valve : Pulmonary valve : Aortic valve : Mitral valve Marfan syndrome(22K) Aortic root dilatationC Aortic regurgitation ( Mitral regurgitation and Mitral valve prolapse ( aneurysms(7K) Aortic aneurysm and Aortic dissection Tokyo Medical University Home Pediatrics Home Genetics Home

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