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Marfan Syndrome:     more books (39)

Marfan Syndrome Mitral Valve Prolapse and the Marfan Syndrome by Richard B. Devereux, 1997-11 Marfan syndrome: A pamphlet for the ophthalmic and optometric professions by Barrie Jay, 1994 A bibliography on the Marfan syndrome and associated disorders by Elizabeth Lieber Fox, 1986 Lincoln did not have the Marfan syndrome: Documented evidence by John Lattimer, 1981 A Dental and cytogenetic study of the Marfan syndrome by Jim D Webb, 1966 Marfan Syndrome: A Primer for Clinicians and Scientists (Medical Intelligence Un by Maurice Godfrey Peter N. Robinson, 2004-01-01 Marfan Syndrome: Emergency Diagnosis and Treatment of Aortic Dissection by Diane Rust, 1998-09 The Marfan syndrome Marfan Syndrome: A Guide for Teens by National Marfan Foundation, 2006 The Physical Lincoln Complete by John G. Sotos, 2008-09-26

lists with details

41. Marfan Syndrome
    marfan syndrome information and resources, links to national and international support groups, clinics with genetic counselors and geneticists.  
    http://www.kumc.edu/gec/support/marfan.html
    
    Extractions: Canadian Marfan Association , includes Similar Disorders to Marfan Syndrome [Beals Congenital Contractual Arachnodactyly), Ehlers Danlos, Hajdu Cheney] Marfan Network Japan Pomagamy chorym z Zespolem Marfana i ich rodzinom , Marfan Association Poland Other Sites: Stanford University Center for Marfan Syndrome Adult Congenital Heart Network , Canadian Adult Congenital Heart Network, Toronto Congenital Cardiac Centre for Adults, and International Society Of Adult Congenital Cardiac Disease Marfan Syndrome Web Site , individual with Marfan Syndrome Clinical Operational Research Unit , University College London, includes Marfan Syndrome Survey, TYWChow , and Timing of Elective Aortic Root Replacement in the Marfan Syndrome: Computerized decision support alt.support.marfan

42. Marfan Syndrome
    Online chapter from The Merck Manual of Medical Information.  
    http://www.merck.com/mrkshared/mmanual_home2/sec23/ch279/ch279c.jsp

43. MedlinePlus: Marfan Syndrome
    Clinical Trials; ClinicalTrials.gov marfan syndrome (National Genetics; Genetics Home Reference marfan syndrome (National Library of Medicine)  
    http://www.nlm.nih.gov/medlineplus/marfansyndrome.html
    
    Extractions: Also available in: Spanish Marfan Syndrome (Mayo Foundation for Medical Education and Research) Patient Guide to Marfan Syndrome (Johns Hopkins Dept. of Orthopaedic Surgery) What is Marfan Syndrome? (Dolan DNA Learning Center) Diagnosis/Symptoms About Marfan Syndrome: Diagnosis (National Marfan Foundation) Treatment Heart Surgery for Marfan Syndrome (Cleveland Clinic Foundation) Specific Conditions Cardiac Concerns (National Marfan Foundation) Ocular Concerns (National Marfan Foundation) Orthopedic Concerns (National Marfan Foundation) Related Issues Marfan Syndrome (American Heart Association) Marfan Syndrome: An Introduction to Related Disorders (National Marfan Foundation) Physical Education and Activity Guidelines (National Marfan Foundation) Clinical Trials ClinicalTrials.gov: Marfan Syndrome

44. MedlinePlus Medical Encyclopedia: Marfan Syndrome
    In sporadic cases, marfan syndrome is believed to result from a spontaneous new mutation. marfan syndrome is caused by mutations in the gene fibrillin1.  
    http://www.nlm.nih.gov/medlineplus/ency/article/000418.htm
    
    Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Pectus excavatum Marfan's syndrome Definition Return to top Marfan syndrome is an inheritable disorder of connective tissue, the tissue that strengthens the body's structures. Disorders of connective tissue affect the skeletal system, cardiovascular system, eyes, and skin. Causes, incidence, and risk factors Return to top 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) 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. How this overgrowth happens is not well understood. Marfan syndrome causes skeletal defects typically seen in a tall, lanky person with long limbs and spider-like fingers (arachnodactyly), chest abnormalities (pectus excavatum or pectus carinatum), curvature of the spine, and a particular set of facial features, including a highly arched palate and crowded teeth.

45. Marfan Syndrome Forum
    Describes the author's personal experiences with this Syndrome and asks readers to share their experiences. Also include links for further research.  
    http://hometown.aol.com/bjthaler6/myhomepage/
    
    Extractions: If you have Marfan Syndrome and might have had some minor or unusual medical condition that is apparently not related to Marfan Syndrome, let me know the specific area you would like me to research for you by sending me an E-mail. Just click the E-mail button at the bottom of this web page. Healthlink,USA

46. Marfan Syndrome / Family VillageLibrary
    An unmoderated forum for anyone interested in the marfan syndrome or related disorders Any topic related to the marfan syndrome and related disorders is  
    http://www.familyvillage.wisc.edu/lib_marf.htm
    
    Extractions: Web: http://www.marfan.org/ The National Marfan Foundation was founded in 1981 by people who have the Marfan syndrome and their families. It is a voluntary organization that has three objectives. To disseminate accurate and timely information about this condition to patients, family members and the health care community. To provide a network of communications for patients and relatives to share experiences, support one another and improve their medical care. And to support and foster research. Canadian Marfan Association (CMA) Web: http://www.marfan.ca/ The Canadian Marfan Association provides accurate, timely information about Marfan Syndrome to help prevent early death and disability, and works to improve the quality of life for Marfan patients in Canada, through comprehensive programs of education, support, and research. They assist patients and their families to live optimally with Marfan Syndrome by forming self-help groups nationally, which will foster improved physical and emotional health and thus enable affected families to seek and follow the most comprehensive health care regime possible.

47. MARFAN SYNDROME: JR FACT SHEET
    This site is an in depth look into the life of someone who has marfan syndrome and what they have learned along the way.  
    http://jrmarfan58.com
    
    Extractions: 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 - 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

48. The Marfan Syndrome MEDSTUDENTS-METABOLIC DISORDERS
    marfan syndrome is discussed in its general aspects. The discussion was based on the clinical manifestations, diagnostic criteria, differential diagnosis  
    http://www.medstudents.com.br/metdis/metdis5.htm
    
    Extractions: Medstudents' Homepage The Marfan syndrome is an inherited disorder of connective tissue. It is characterized by skeletal abnormalities (pectus escavatum, pectus carinatum, scoliosis, high arched palate, tall stature, long arms and long fingers -arachnodactily); ocular abnormalities (characteristic upper dislocation of lens, myopia); ligamentar laxity and cardiovascular abnormalities (aortic dilatation, mitral valve prolapse and sometimes aortic dissection). The disease is due to a mutation on the fibrillin gene. It can be inherited as a autossomal dominant trait. 60% to 70% of affected person have a positive family history. The patients may have diverse clinical manifestations. Thoracic abnormalities may progress as scoliosis during adolescence, or lead to spontaneous pneumothorax. The ocular ectopia of lens usually is in the upper direction and can lead to glaucoma and cataracts. The diagnosis usually is made based on a tall individual with long fingers resembling a spider (arachnodactily), scoliosis or kyphosis, long arms, lens dislocation and mitral valve prolapse that can evolute to mitral regurgitation or aortic regurgitation due to aortic aneurism. Sometimes a ligamentous laxity similar to Ehler Danlos syndrome is observed. The life threatening manifestation is aortic dissection that is related to the size of aortic dilatation. Aortic diameter increases with age, not exceeding the normal range until the third decade. Cardiac abnormalities are the major source of morbidity and mortality.

49. The Marfan Syndrome
    The marfan syndrome has been publicized in sport magazines because of the sudden, The marfan syndrome is an inherited, degenerative disorder of the  
    http://www.hughston.com/hha/a_12_2_4.htm
    
    Extractions: The Marfan Syndrome The Marfan syndrome has been publicized in sport magazines because of the sudden, untimely deaths of Olympic volleyball player Flo Hyman and collegiate basketball player Chris Patton who had this condition. The Marfan syndrome is an inherited, degenerative disorder of the connective tissue, which gives shape and structure to tissues in the body and holds them in place. It affects several organ systems including the ocular system (eyes), the cardiovascular system (heart and blood vessels), and the skeletal system (bones and joints). The condition is considered a syndrome because the physical symptoms occur together frequently enough for a pattern to be recognized. More than 50,000 people in the United States have the Marfan syndrome. Signs and symptoms Because of the physical characteristics that can accompany the Marfan syndrome, the term has been used loosely - and sometimes incorrectly or without evidence - to describe any person who is tall and thin and has long arms and legs. An unsuccessful proposal was made in the 1980s for athletes in the National Basketball Association to undergo testing for the Marfan syndrome. Without conclusive evidence, historians and medical professionals have debated whether Abraham Lincoln had the Marfan syndrome. Diagnosis Diagnosing the Marfan syndrome is difficult because the number and severity of symptoms affecting each person varies. The doctor may first recognize that you demonstrate some symptoms of the disorder when treating you for a dislocated hip, kneecap, or jaw; groin pain due to a hernia; or spontaneous leakage of air from the lungs into the chest cavity.

50. DermAtlas: Online Dermatology Image Library Dermatology Image,Marfan Syndrome,hy
    Comments, The most progressive cardiac lesion in marfan syndrome is Comments, A newborn whose mother has marfan syndrome was noted at birth to have  
    http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=2131942276

51. Marfan Syndrome
    marfan syndrome is an inheritable disorder of connective tissue (which adds strength to the body s structures) that affects the skeletal system, system,  
    http://www.healthcentral.com/ency/408/000418.html
    
    Extractions: Dr. Dean TV Specials Newsletters Home ... Health Tools Search Choose a Health Topic * All Health Topics * Acne Addictions AIDS/HIV Alcohol Abuse Allergies Alternative Medicine Alzheimer's Arthritis Asthma Attention Deficit Disorder (ADHD) Backache Bipolar Affective Disorder Birth Control Blood Blood Pressure Bone/Joint/Tendon Bowel Brain Breast cancer Cancer Cerebral Palsy Cholesterol Cramps Crohn's Disease Cysts Dental/Oral Depression Diabetes Diet, Fitness, Looks Disabled/Special Needs Drug Abuse Ear/Nose/Throat Eating/Appetite Eczema Encephalitis Eye/Vision Fatigue Fever Flu Food Poisoning Foot Gallbladder Gastrointestinal Genetic/Congenital GERD/Heartburn Hair Loss Hair/Scalp Headache Hearing Heart Disease, Stroke Heat/Sunstroke Hepatitis Hernia Herpes High Blood Pressure Hormonal Immune Disorders Immunizations/Vaccines Impotence Incontinence/Bladder Infections Injuries Kidney/Urinary Kids Learning Disabilities Liver Lung Cancer Men Menopause, Postmenopause Migraine Mobility/Balance Multiple Sclerosis Muscle Neural Nosebleeds Pain Parasites Pituitary PMS Pregnancy Prostate Cancer Prostate Disorders Psoriasis Psychological Raynaud's Disease Respiratory Reye Syndrome Rheumatoid Arthritis Schizophrenia Seniors Sensory Sexually Transmitted Disease Skin Sleep Speech Disorders Spinal Thyroid Trauma Weight Loss Women Yeast Infections

52. Marfan Syndrome: Definition And Much More From Answers.com
    Mar·fan syndrome ( mär fan ) n. A hereditary disorder principally affecting the connective tissues of the body, manifested in varying degrees by.  
    http://www.answers.com/topic/marfan-syndrome
    
    Extractions: n. A hereditary disorder principally affecting the connective tissues of the body, manifested in varying degrees by excessive bone elongation and joint flexibility and by abnormalities of the eye and cardiovascular system. Wikipedia Marfan syndrome Marfan syndrome is a connective tissue disorder, affecting many structures, including the skeleton lungs eyes heart and blood vessels . It is named for the French pediatrician Antoine Marfan , who first described it in . The disease is characterized by unusually long limbs Marfan syndrome is an autosomal dominant disorder that has been linked to the FBN1 gene on chromosome encodes a protein called fibrillin , which is essential for the formation of elastic fibres found in connective tissue. Marfan's Syndrome is associated with incomplete penetrance, therefore not all persons carrying the mutation develop the disease. Without the structural support provided by fibrillin, many connective tissues are weakened, which can have severe consequences on support and stability. A related disease has been found in

53. Marfan Syndrome
    Thoene, Jess G. marfan syndrome. In Physician s Guide to Rare Diseases. National Marfan Foundation, 382 Main Street, Port Washington, NY, 11050,  
    http://www.healthatoz.com/healthatoz/Atoz/ency/marfan_syndrome.jsp

54. About - Marfan Syndrome.
    marfan syndrome is a rare hereditary disorder that causes connective tissue For people with marfan syndrome, weak connective tissue causes problems of  
    http://www.orthop.washington.edu/uw/marfansyndrome/tabID__3376/ItemID__40/Articl
    
    Extractions: Home Site Map Contact Us Links ... All Articles Marfan Syndrome. University of Washington, Seattle Last updated Thursday, December 23, 2004 Basics of marfan syndrome Marfan syndrome is a rare hereditary disorder that causes connective tissue to be weaker than normal. Connective tissue is the most abundant tissue in the body. It supports and protects various other tissues, is a vital component of all organs in the body, and provides strength and elasticity to blood vessels. Therefore, a disorder of connective tissue can cause a variety of abnormal conditions. For people with Marfan syndrome, weak connective tissue causes problems of the skin, muscles, ligaments, heart, eyes, blood vessels, and bones.

55. HONselect - Marfan Syndrome
    Français, Syndrome de Marfan, Arachnodactylie - Dolichosténomélie - Marfan, syndrome - Maladie de Marfan. Deutsch, Marfan-Syndrom, - Arachnodaktylie  
    http://www.hon.ch/HONselect/RareDiseases/C05.116.099.674.html

56. Introduction: Marfan Syndrome - WrongDiagnosis.com
    Introduction to marfan syndrome as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.  
    http://www.wrongdiagnosis.com/m/marfan_syndrome/intro.htm
    
    Extractions: Marfan syndrome: Marfan syndrome is a heritable condition that affects the connective tissue. The primary purpose of connective tissue is to hold the body together and provide a framework for growth and development. In Marfan syndrome, the connective tissue is defective and does not act as it should. Because connective tissue is found throughout the body, Marfan syndrome can affect many body systems, including the skeleton, eyes, heart and blood vessels, nervous system, skin, and lungs. Researching symptoms of Marfan syndrome: Further information about the symptoms of Marfan syndrome is available including a list of symptoms of Marfan syndrome , or alternatively return to research other symptoms in the symptom center Treatments for Marfan syndrome: Various information is available about treatments available for Marfan syndrome current research about Marfan syndrome treatments , or research treatments for other diseases.

57. Marfan Syndrome
    Detailed information on marfan syndrome, including causes, diagnosis, and treatment.  
    http://www.healthsystem.virginia.edu/uvahealth/peds_cardiac/marfan.cfm
    
    Extractions: [ Skip Navigation ] Topics Adolescent Medicine Allergy/Asthma/Immunology Blood Disorders Burns Cancer Common Injuries/Poison Tips Craniofacial Anomalies Dermatology Diabetes/Endo/Metabolism Eye Care Genitourinary/Kidney High-Risk Newborn High-Risk Pregnancy Infectious Diseases Medical Genetics Mental Health Nervous System Disorders Normal Newborns Oral Health Orthopaedics Pediatric Surgery Respiratory Disorders Terminal Illness in Children Transplantation Search This Site Marfan syndrome is a disorder involving the body's connective tissue. Connective tissue has many important functions, including the following: assisting with growth and development of the body's cells, both before and after birth facilitating the passage of light through the eye A defective (FBN1) gene associated with Marfan syndrome affects the formation of a protein in connective tissue called fibrillin, which impacts the integrity of many organs and structures in the body. Organs and body systems that can be impacted include, but are not limited to, the following:

58. Marfan Syndrome
    marfan syndrome is a disorder that affects the body s connective tissue. This causes problems in many systems of the body, but especially the heart, eyes,  
    http://kidshealth.org/kid/health_problems/birth_defect/marfan.html
    
    Extractions: Evan couldn't wait for school to begin. All summer long, he'd looked forward to trying out for the basketball team. He'd be a natural, everyone told him. At 14, he pretty much towered over his classmates. But when the time came for his sports physical, the doctor noticed some things about Evan that needed a closer look. It wasn't just that Evan was really tall for his age - 6 feet and 1 inch, to be exact - but his arms, legs, and fingers were very long and thin and his chest had kind of a caved-in look. He also wore glasses for myopia (say: my- o -pee-uh), or nearsightedness, which means he had trouble seeing things that were far away. The doctor told Evan's parents that he couldn't give Evan the OK to try out until Evan had a few medical tests. Why? Because the doctor suspected that Evan might have a disorder called Marfan syndrome. What Is Marfan Syndrome? Named after Antoine Marfan, the French doctor who discovered it in 1896, Marfan syndrome is a disorder that affects the body's connective tissue (say: kuh- nek -tiv tih -shoo). Connective tissue is found everywhere in the body. Think of it as a type of "glue" that helps support all of your organs, blood vessels, bones

59. Marfan Syndrome - MayoClinic.com
    marfan syndrome, a connective tissue disorder, can affect almost every part of your body, including your heart, eyes and ligaments.  
    http://www.mayoclinic.com/invoke.cfm?id=DS00540

60. Marfan Syndrome
    marfan syndrome is an inherited disorder that affects primarily the eyes, the heart, marfan syndrome is inherited in an autosomal dominant manner.  
    http://www.uth.tmc.edu/schools/med/imed/med_gen/marfan.htm
    
    Extractions: Marfan syndrome is inherited in an autosomal dominant manner. If a person is affected with Marfan syndrome, they face a 50% chance of passing on the disease with every pregnancy. In 1 in 4 of all cases of Marfan syndrome, the parents are not affected. In these cases, the condition arises in the affected person because of a spontaneous or new mutation in the egg or the sperm of one of the parents. The disorder is fully penetrant, meaning that unaffected relatives of a Marfan patient will not pass the disorder on to their children. What symptoms are involved?

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