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         Marfan Syndrome:     more books (39)
  1. The Official Patient's Sourcebook on Marfan Syndrome
  2. Marfan Syndrome: A Primer for Clinicians and Scientists (Medical Intelligence Unit)
  3. Marfan Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-01-23
  4. The Marfan Syndrome by Reed E. Pyeritz, Cheryll Gasner, 1994-05
  5. An Overview of the Marfan Syndrome by Elizabeth L. Fox, 1989-06
  6. 21st Century Ultimate Medical Guide to Marfan Syndrome - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-05-23
  7. Marfan Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  8. Questions and answers about Marfan Syndrome. (Health Topics).(Pamphlet): An article from: Pamphlet by: Nat'l Inst. of Arthritis and Musculoskeletal & Skin Diseases
  9. Questions and Answers About Marfan Syndrome.(Pamphlet): An article from: Pamphlet by: Nat'l Inst. of Arthritis and Musculoskeletal & Skin Diseases
  10. 21st Century Complete Medical Guide to Marfan Syndrome: Authoritative Government Documents, Clinical References, and Practical Information for Patients and Physicians by PM Medical Health News, 2004-05
  11. Marfan Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Rebecca, PhD Frey, 2006
  12. The Marfan Syndrome: Physical Activity Guidelines for Physical Educators, Coaches & Physicians by Thomas J. Romeo, 1992-01
  13. Gale Encyclopedia of Medicine: Marfan syndrome by Rebecca J. Frey PhD, 2002-01-01
  14. Marfan syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Science, 3rd ed.</i> by Bryan Cobb, 2004

81. THE MERCK MANUALSECOND HOME EDITION, Marfan Syndrome In Ch. 279
marfan syndrome. marfan syndrome is a rare disorder of connective tissue,resulting in abnormalities of the eyes, bones, heart, and blood vessels.
http://www.merck.com/mrkshared/mmanual_home2/sec23/ch279/ch279c.jsp

82. Cardiovascular Disorders - Marfan Syndrome
marfan syndrome What is marfan syndrome? marfan syndrome is a disorderinvolving the body s connective tissue. Connective tissue
http://www.chkd.org/Cardiology/marfan.asp
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For a doctor who specializes in this topic, click here. Marfan Syndrome What is Marfan syndrome?
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 supporting tissues in the body acting as an adhesive to hold certain tissues together protecting joints 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:

83. Marfan Syndrome
marfan syndrome and Aortic Disease. Introduction to the marfan syndrome.The marfan syndrome is a connective tissue disorder affecting
http://www.csmc.edu/5230.html

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Marfan Syndrome and Aortic Disease Additional Aorta-Related Resources from Cedars-Sinai Introduction to the Marfan Syndrome The Marfan syndrome is a connective tissue disorder affecting multiple areas of the human body to varying degrees. Connective tissue is prevalent throughout the body, and consequently areas such as the skeleton, skin, lungs, eyes, blood vessels and heart may all be impacted. Greater understanding of the underlying cause of this syndrome continues to emerge through genetic research currently in progress at various centers. While there is no cure for this condition at this time, continuous advancement in medical and surgical treatment options has increased both the length and quality of life of those affected by it. Back to Top The Marfan Syndrome and Aortic Disease The abnormal aortic tissue associated with Marfan syndrome is prone to aortic dissection or aneurysmal rupture, which are life threatening. Therefore, the single most important factor in the survival of Marfan syndrome patients is the safe and elective resection of the most vulnerable portion of the aorta, most commonly the aortic root.

84. The DRM WebWatcher: Marfan Syndrome
A Disability Resources Monthly guide to the best online resources about Marfansyndrome. Check these sites for information about marfan syndrome.
http://www.disabilityresources.org/MARFAN.html
Home Subjects States Librarians ... Contact Us The DRM WebWatcher Marfan Syndrome Updated 1/2004 A B C D ... About/Hint/Link
Marfan syndrome is a rare hereditary disorder that affects the connective tissue, and can cause excessive height and problems of the the skeletal system, eyes, lungs, blood vessels and heart. Check these sites for information about Marfan syndrome.
Marfan Syndrome Info Ring
A network of personal web sites by and about people with Marfan syndrome.
The National Marfan Foundation
The Foundation's web site includes informative and authoritative publications about Marfan syndrome (including the comprehensive Marfan Syndrome Resource Manual ), a quarterly newsletter, an extensive list of support groups around the world, links to related sites, and short profiles of people with Marfan syndrome to contact.
Related Subjects
Arthritis
Growth Disorders
Resources in your state
(c) 1997-2000 Disability Resources, inc.

85. A To Z Encyclopedia Topic: Marfan Syndrome
Clinical Services. marfan syndrome. What is marfan syndrome? marfan syndrome isa disorder involving the body s connective tissue. What causes marfan syndrome?
http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Marfan syndrome

86. Marfan Syndrome
What Is marfan syndrome? The Marfan group. It is estimated that over5,000 people in the United Kingdom have marfan syndrome. A
http://www.c-r-y.org.uk/marfan_syndrome.htm
CRY Cardiac Risk in the Young home about cry contacts medical info ... news Medical Information Hypertrophic Cardiomyopathy (HCM) Arrhythmogenic Right Ventricular Cardiomyopathy ARVC) Dilated Cardiomyopathy (DCM) Myocarditis ... ndocardial Fibroelastosis (EFE), Tachycardia
Marfan Syndrome
What causes Marfan Syndrome?
How can you recognise Marfan Features

Salient Features

What Treatment Is Available?
...
Further Information
What Is Marfan Syndrome?
The Marfan Syndrome is an inherited disorder of connective tissue which affects many organ systems, including the skeleton, lungs, eyes, heart and blood vessels. This condition, first described by Dr Marfan in 1896, can affect both boys and girls of any race or ethnic group. It is estimated that over 5,000 people in the United Kingdom have Marfan Syndrome. A syndrome is a collection of physical features which, when they occur together, enable a physician to recognise a certain condition. Most affected people will not show all the signs and complications of Marfan Syndrome. Top of the page
What Causes Marfan Syndrome?

87. BHF Heart Health - Heart Terms: Marfan Syndrome
Magnetic Resonance Imaging to Myocardium. Magnetic Resonance Imaging. Marfansyndrome. Mechanical valve. Mitral stenosis. Mitral valve prolapse. Mitral valve.
http://www.bhf.org.uk/hearthealth/index.asp?secID=1&secondlevel=74&thirdlevel=26

88. Marfan, Syndrome : Sites Et Documents Francophones
Translate this page Arborescence(s) du thesaurus MeSH contenant le mot-clé Marfan, syndromemarfan syndrome Marfan, syndrome de Par Pr Parc (Le) JM.
http://www.chu-rouen.fr/ssf/pathol/marfansyndrome.html
Marfan, syndrome Menu général CISMeF Synonyme(s) MeSH Arachnodactylie ; Dolichosténomélie ; Syndrome Marfan
Arborescence(s) Marfan, syndrome Marfan syndrome
appareil cardiovasculaire, maladies
appareil locomoteur, maladies maladies et malformations congénitales, héréditaires et néonatales maladies peau et tissu conjonctif Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources :
Qualificatifs : illustration médicale patient

89. SupportPath.com: Marfan Syndrome
SupportPath.com, marfan syndrome. Also called Marfan s Syndrome. Other Interest None Listed. Clinical Trials Research on marfan syndrome
http://www.supportpath.com/sl_m/marfan_syndrome.htm
Marfan Syndrome
Also called: Marfan's Syndrome Other topics of interest on SupportPath.com:
Mitral Valve Prolapse Syndrome
Scoliosis Visual Impairment About Us ... here
Online Communities / Message Boards...
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  • alt.support.marfan

90. DIRC Fact Sheet - Marfan Syndrome
marfan syndrome. Fact Sheet. Marfan Support and Information (NSW). Email mailtomail@marfan.net.auWeb http//www.marfan.net.au/. What is marfan syndrome?
http://www.dircsa.org.au/pub/docs/marfan.htm
MARFAN SYNDROME Fact Sheet Marfan Support and Information (NSW) Email: mailto:mail@marfan.net.au
Web: http://www.marfan.net.au/ What is Marfan Syndrome? Marfan Syndrome is an inheritable disorder of the connective tissue that affects many organ systems, including the skeleton, lungs, eyes, heart and blood vessels. The condition affects both men and women of any race or ethnic group. What medical problems are associated with Marfan Syndrome? The Cardiovascular System The most serious problems associated with Marfan Syndrome involve the cardiovascular system. The two leaflets of the mitral valve may billow backwards when the heart contracts (mitral valve prolapse). This can lead to leakage of the mitral valve or irregular heart rhythm. In addition, the aorta, the main artery carrying blood away from the heart, is generally wider and more fragile in patients with Marfan Syndrome. This widening is progressive and can cause leakage of the aortic valve or tears (dissection) in the aorta wall. When the aorta becomes greatly widened, or tears, surgical repair is necessary. The Skeleton Skeletal manifestations common in people with Marfan Syndrome include curvature of the spine (scoliosis), loose jointedness and disproportionate growth usually, but not always, resulting in tall stature.

91. Marfan Syndrome
marfan syndrome. Pectus involved. How Is marfan syndrome Diagnosed?There is as yet no single test for identifying marfan syndrome.
http://www.users.bigpond.com/conover/PE/marfan.htm
Marfan Syndrome
Pectus excavatum and carinatum are just two of a huge collection of conditions resulting from disordered connective tissue formation. Connective tissue includes bone, cartilage, tendons, ligaments and elastic tissues, among others. When something goes wrong during formation, the resulting tissue lacks the qualities of either strength or elasticity it should have, and its growth may be quite abnormal. Although medical science has located genes where errors can occur resulting in connective tissue disorder no underlying circumstance that causes it to happen in the first place has been identified. Such disorders may affect just a few or many areas of the body at once. pectus as a symptom is Marfan Syndrome . It's suggested that Marfan may be present in one of every 5000 to 10,000 births. And if a parent has the condition, chances are 50/50 of a child having the same tendency. Certainly, while "isolated" PE or PC do indeed reflect a problem with connective tissue formation, not all people with pectus have the full range of other connective tissue changes that characterise Marfan. But because Marfan can involve weakness of major blood vessels, with a potential for rupture

92. Cardiovascular Disorders - Marfan Syndrome
marfan syndrome. What is marfan syndrome? Marfansyndrome is a disorderinvolving the body s connective tissue. What causes marfan syndrome?
http://www.musckids.com/health_library/cardiac/marfan.htm

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Cardiovascular Disorders
Marfan Syndrome
  • assisting with growth and development of the body's cells, both before and after birth supporting tissues in the body acting as an adhesive to hold certain tissues together protecting joints facilitating the passage of light through the eye heart and major blood vessels lungs skeletal system spinal cord eyes skin
    prolapse - an abnormality of the valve between the left atrium and left ventricle of the heart that causes backward flow of blood from the left ventricle into the left atrium. arrhythmia (or dysrhythmia) - a fast, slow, or irregular heartbeat. aortic regurgitation - backwards leakage of blood from the aorta, through a weakened aortic valve, and into the left ventricle, resulting in stress in the left heart and inadequate blood flow to the body. aortic dissection - weakening of the layers inside the aorta, which can result in tears in the aortic wall and leakage of blood into the chest or abdomen; a medical emergency.
    heart and blood vessels
    • dilation of the aorta leakage of the aortic valve (aortic regurgitation) tears in the aorta (aortic dissection)
    skeletal
    • deformities of the breastbone scoliosis - a lateral, or sideways curvature and rotation of the back bones (vertebrae), giving the appearance that the person is leaning to one side.

93. Marfan Syndrome
marfan syndrome. What is marfan syndrome? It affects men, women , andall racial and ethnic groups equally. What causes marfan syndrome?
http://www.uth.tmc.edu/schools/med/imed/med_gen/marfan.htm
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Aortic Aneurysms and Aortic Dissections

Marfan Syndrome

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Marfan Syndrome
What is Marfan syndrome?
Marfan syndrome is an inherited disorder that affects primarily the eyes, the heart, blood vessels (cardiovascular systems), and the bones and joints (skeletal system). The disorder was first described by a French pediatrician, Antoine Marfan in 1896 and bears his name. How is it inherited?
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?

94. Marfan's Syndrome -- ECureMe.com
, symptoms, diagnoses, treatment and other information with a couple of similar disorders for comparison.......
http://www.ecureme.com/emyhealth/data/Marfan's_Syndrome.asp
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Marfan's Syndrome
more about Marfan's Syndrome

  • Marfan's Syndrome is an inherited (autosomal dominant) disorder, caused by a defective gene involved with the production of fibrillin. Fibrillin makes up part of connective tissue in the body, such as the blood vessels, eye lenses, and ligaments.
    Patient has long, thin arms, legs, fingers, and toes.

95. Booklets2000
Please help us by taking these surveys and explain your experiences with Connective Tissue Disorders like EhlersDanlos syndrome, marfan's syndrome, Stickler Involved syndrome, and Fibromyalgia.
http://www.angelfire.com/il2/booklets2000/index.html
var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded"
WHO HAS IT? Connective Tissue Disorders do not appear to favor one set of genes over another. People from every age, gender, race, religion, and hemisphere are candidates. DOES IT EFFECT YOUR LIFE? Can people with C.T.D. still contribute? You bet they can!
with Connective Tissue Disorder. LIFE DOES GO ON . . . Focusing on the pace – not on the hurdles – makes life more worthwhile. There are ways to improve your condition:
"Quality of Life" can always be improved!
Medical breakthroughs,
personal support systems,
new medications and treatments,
– appear on the scene every day. Review advice from others who share your
symptoms. Share your thoughts
and experiences. Find a good doctor in your area. Take Survey

96. Association Française De Syndrome De Marfan
Informer, aider et soutenir les personnes atteintes du syndrome et leur famille.
http://www.geocities.com/vivremarfan/
Cette page utilise des cadres, mais votre navigateur ne les prend pas en charge.

97. Accueil
  Accueil Le syndrome de marfan, r©seau de sp©cialistes, oeuvrer pour une vie confortable et de longue dur©e, le r´le des associations et du conseil scientifique de l'ASMMA
http://www.orpha.net/associations/ASMAA/ASMAA.html
Accueil
Accueil Le syndrome de Marfan Réseau de spécialistes Oeuvrer pour une vie confortable et de longue durée ... Nous contacter
ASMAA
Association syndrome de Marfan Les amis d'Antoine Reconnue d'intérêt général Siège social C/O FNAMOC CHU Sainte-Anne 1, rue Cabanis 75674 Paris cedex 14 Secrétariat 23 Rue de la Libération 95880 ENGHIEN LES BAINS FRANCE Tél - Fax : 01 39 64 99 69 E-mail : jtihierr@free.fr
(c) Annette BELLONCLE Auteur : Mme Annette BELLONCLE Date de création de la page : 14/01/2003 Date de dernière mise à jour : 14/01/2003

98. Doctors Try To Unravel The Marfan Mystery
CNN
http://cnn.com/2002/HEALTH/conditions/04/22/marfan.syndrome.ap/index.html

99. Hypermobility Forum For People With Marfan, EDS
This is a moderated discussion board for Hypermobility syndrome, marfan, and EhlersDanlos. Includes personal experiences, traditional and alternative treatment, and pain.
http://marge.com/hypermobility/
Welcome to Hypermobility Forum for people with Marfan, EDS
Your browser does not support Frames. Therefore, navigation of Hypermobility Forum for people with Marfan, EDS will not be aided by having a menu present at all times. The following is the menu made available to those with a frame-compatible browser: Top (Index) Instructions Formatting Troubleshooting ... User Profile Administration (Requires Frames)
Click Here to Start

100. OurHospitals
Definition, description, symptoms and even treatments are covered here. There is also a list of questions one should ask their doctor.
http://www.etenet.com/Apps/Library/Corporate.asp?ID=607

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