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Marfan syndrome

Marfan syndrome is a connective tissue disorder characterized by unusually long limbs. The disease also affects other bodily structures—including the skeleton, lungs, eyes, heart and blood vessels—in less obvious ways. It is named for Antoine Marfan, the French pediatrician who first described it in 1896. more...

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Medicines

Genetics

Marfan syndrome is an autosomal dominant disorder that has been linked to the FBN1 gene on chromosome 15. FBN1 codes for a protein called fibrillin , which is essential for the formation of elastic fibres found in connective tissue. Marfan 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 mice, and it is hoped that the study of mouse fibrillin synthesis and secretion, and connective tissue formation, will further our understanding of Marfan syndrome in humans.

Although genetic testing is available, a diagnosis is usually made solely on clinical findings. Most individuals with Marfan syndrome have another affected family member, but about 30 percent of cases are due to genetic mutations (de novo). Genetic counseling is available for families who may be at risk for Marfan syndrome.

Estimates indicate that perhaps 1 in 10,000 people (0.01 percent of the population) has Marfan syndrome. There is no cure, but effective treatment allows many people with the disorder to live normally. It affects all races and sexes equally.

Symptoms

The most serious conditions associated with Marfan syndrome primarily involve the cardiovascular system. Marfan syndrome may cause leakage of the mitral or aortic valves that control the flow of blood through the heart. This may produce shortness of breath, an irregular pulse, and undue tiredness. Another complication is aortic aneurysm.

Marfan syndrome sufferers may grow to larger than normal height, and typically have long, slender limbs and fingers. Sometimes the fingers have a long, thin, spidery appearance known as arachnodactyly. In addition to affecting height and limb proportions, Marfan syndrome may produce other skeletal symptoms. Curvature of the spine (scoliosis) is a common problem, as is abnormal indentation (pectus excavatum) or protrusion (pectus carinatum) of the sternum. These symptoms may in turn cause unusual pressure on the heart and lungs. Other symptons include; abnormal joint flexibility, high palates, flat feet, stooped shoulders, and dislocation of the optic lens.

Nearsightedness or myopia is a common condition associated with Marfan syndrome. In addition, the weakening of connective tissue often causes detachment of the retina and/or displacement of the lens in one or both eyes.

Treatment

The heart conditions related to Marfan syndrome may not necessarily produce obvious symptoms. As a result, regular checkups by a cardiologist are needed to monitor cardiovascular health. Potential problems may be detected through echocardiography, which involves the use of ultrasound to study the heart valves and the aorta. Beta blockers have been used to control some of the complications such as aortic aneurysms. If the dilation of the aorta threatens to lead to rupture a composite aortic valve and graft may be implanted. Although aortic graft surgery is a serious undertaking it usually results in a good outcome and a satisfactory quality of life. Elective aortic valve/graft surgery is usually considered when aortic dilatation reaches 50 millimeters, but each case needs to be specifically evaluated by a qualified cardiologist. New valve-sparing surgical techniques are becoming more common. Rupture of the aorta, or aortic dissection, is the most common cause of sudden death among Marfan syndrome sufferers.

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Marfan Syndrome : A Primer for Clinicians and Scientists (Medical Intelligence Unit) $80.00 The Official Patient's Sourcebook on Marfan Syndrome $28.24
Marfan syndrome alert. (Bits & Pieces). : An article from: Palaestra $5.95 Marfan Syndrome: Identification And Management. : An article from: MedSurg Nursing $5.95
Gale Encyclopedia of Medicine : Marfan syndrome $5.99 Acne fulminans in Marfan syndrome.(CASE REPORTS) : An article from: Journal of Drugs in Dermatology $5.95
Cardiovascular Aspects of Marfan Syndrome $55.90 The Marfan Syndrome $17.95
Marfan Syndrome: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References $39.41 Case study: A 44 old female presenting with Marfan's syndrome : An article from: Synergy $10.00

Acne fulminans in Marfan syndrome
Abstract We report on a 12-year-old boy suffering from acne fulminans in combination with Marfan syndrome. The trigger for acne induction seemed to ...
Marfan syndrome
Marfan syndrome (or Marfan's syndrome) is an inherited disease that affects the connective tissue within the body. This results in a variety of skeletal ...
Relationship between Craniofacial abnormalities and sleep-disordered breathing in Marfan's syndrome - clinical investigations
Objectives: To examine the prevalence and nature of craniofacial abnormalities in patients with Marfan's syndrome and to investigate the relationship ...
Questions and answers about Marfan Syndrome - Health Topics - Pamphlet
This booklet answers general questions about Marfan syndrome. It describes the characteristics of the disorder, the diagnostic process, and ways to manage symptoms. If you have additional questions
Infantile Marfan Syndrome—A 5 Week Old With Unusual Pulmonary Manifestations
Sharon Calaman MD, A Jacobs MD, G Crooke MD, A Racine MD, PhD, J Glickstein MD, J Weingarten-Arams MD FCCP--Department of Pediatrics, Divisions of Pediatric ...
Revised Booklet on the Marfan Syndrome
The National Marfan Foundation has recently released the fifth revised edition of "The Marfan Syndrome," a complete resource on this genetic disorder ...
Marfan's syndrome and surgical repair of ascending aortic aneurysms - Home Study Program article with examination, answer sheet and learner evaluation
Patients with Marfan's syndrome require periodic examinations and echocardiograms to measure aortic root diameters. Enlarged diameters are an indication ...
Marfan Syndrome Guide - Brief Article - Statistical Data Included
The fifth edition of "The Marfan Syndrome" covers heredity, diagnosis, symptoms, treatment, psychosocial issues, health insurance, and research. Single ...

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