0
What is the most common surgical procedure used to repair the aorta of a Marfan syndrome patient?
GaleEncyofMedicine
As of 2000, the most common surgical treatment involves replacing the patient's aortic valve and several inches of the aorta itself with a composite graft, which is a prosthetic heart valve sewn into one end of a Dacron tube.
Wiki User
∙ 13y ago
Add your answer:
Earn +20 pts
What are the causes for deviated nasal septum?
Can you explain how it is also present in about 11% of patients with Marfan syndrome?
Causes for inlarged aorta what does this mean?
There are several reasons an aorta could be enlarged. Significant ones include hypertension, diseases of elastic tissue (including Marfan's syndrome), and syphilitic aortitis (due to long-standing infection with syphilis)
What are the 100 forms of arthritis?
Forms of arthritis and associated diseasesLupus, Lyme Disease, Adult Onset Still's Disease, Marfan Syndrome, Ankylosing Spondylitis, Mycotic Arthritis, Osgood-Schlatter Disease, Osteitis Deformans, Aseptic Necrosis, Osteoarthritis, Avascular Necrosis, Osteonecrosis, Basal Joint Arthritis, Osteoporosis, Behcet's Disease, Bursitis, Paget's Disease of Bone, Carpal Tunnel Syndrome, Palindromic Rheumatism, Celiac Disease, Polyarteritis Nodosa, CMC Arthritis, Polymyalgia Rheumatica, Complex Regional Pain, Polymyositis, Costochondritis, Pseudogout, Psoriatic Arthritis, Crohn's Disease, Raynaud's phenomenon, Degenerative Joint Disease, Dermatomyositis, Reiter's Syndrome, Discoid Lupus, Erythematosus, Ehlers-Danlos Syndrome, Rheumatic Fever, Eosinophilic Fasciitis, Rheumatoid Arthritis, Felty Syndrome, Scleroderma, Fibro myalgia, Septic Arthritis, Fifth Disease, Sjogren's Syndrome, Forestier Disease, Somatotroph Adenoma, Fungal Arthritis, Spinal Stenosis, Gaucher Disease, Takayasu Arteritis, Giant Cell Arteritis, Temporal Arteritis Gonococcal Arthritis, Tendonitis, Gout, Tietze's Syndrome, Henoch-Schonlein Purpura, TMJ / TMD, Infectious Arthritis, Tuberculous Arthritis. Inflammatory Bowel Disease, Ulcerative Colitis, Joint Hyper mobility, Vasculitis, Juvenile Arthritis, Viral Arthritis, Kawasaki Disease, Wegener's Granulomatosis, Legg-Calve-Perthes Disease,
What are two types of arthritis?
There are many types of arthritis: Achilles tendinitis, Achondroplasia, Acromegalic arthropathy, Adhesive capsulitis, Adult onset Still's disease, Amyloidosis, Ankylosing spondylitis, Anserine bursitis, Avascular necrosis, Behcet's syndrome, Bicipital tendinitis, Blount's disease, Brucellar spondylitis, Bursitis, Calcaneal bursitis, Calcium pyrophosphate dihydrate (CPPD), crystal deposition disease, Caplan's syndrome, Carpal tunnel syndrome, Chondrocalcinosis, Chondromalacia patellae, Chronic synovitis, Chronic recurrent multifocal osteomyelitis, Churg-Strauss syndrome, Cogan's syndrome, Corticosteroid-induced osteoporosis, Costosternal syndrome, CREST syndrome, Cryoglobulinemia, Degenerative joint disease, Dermatomyositis, Diabetic finger sclerosis, Diffuse idiopathic skeletal hyperostosis (DISH), Discitis, Discoid lupus erythematosus, Drug-induced lupus, Duchenne's muscular dystrophy, Dupuytren's contracture, Ehlers-Danlos syndrome, Enteropathic arthritis, Epicondylitis, Erosive inflammatory osteoarthritis, Exercise-induced compartment syndrome, Fabry's disease, Familial Mediterranean fever, Farber's lipogranulomatosis, Felty's syndrome, Fibromyalgia, Fifth's disease, Flat feet, Foreign body synovitis, Freiberg's disease, Fungal arthritis, Gaucher's disease, Giant cell arteritis, Gonococcal arthritis, Goodpasture's syndrome, Gout, Granulomatous arteritis, Hemarthrosis, Hemochromatosis, Henoch-Schonlein purpura, Hepatitis B surface antigen disease, Hip dysplasia, HIV induced inflammatory arthritis, Hurler syndrome, Hypermobility syndrome, Hypersensitvity vasculitis, Hypertrophic osteoarthropathy, Immune complex disease, Impingement syndrome, Jaccoud's arthropathy, Juvenile ankylosing spondylitis, Juvenile dermatomyositis, Juvenile rheumatoid arthritis, Kawasaki disease, Kienbock's disease, Legg-Calve-Perthes disease, Lesch-Nyhan syndrome, Linear scleroderma, Lipoid dermatoarthritis, Lofgren's syndrome, Lyme disease, Malignant synovioma, Marfan's syndrome, Medial plica syndrome, Metastatic carcinomatous arthritis, Mixed connective tissue disease (MCTD), Mixed cryoglobulinemia, Mucopolysaccharidosis, Multicentric reticulohistiocytosis, Multiple epiphyseal dysplasia, Mycoplasmal arthritis, Myofascial pain syndrome, Neonatal lupus, Neuropathic arthropathy, Nodular panniculitis, Ochronosis, Olecranon bursitis, Osgood-Schlatter?s disease, Osteoarthritis, Osteochondromatosis, Osteogenesis imperfecta, Osteomalacia, Osteomyelitis, Osteonecrosis, Osteoporosis, Overlap syndrome, Pachydermoperiostosis, Paget's disease of bone, Palindromic rheumatism, Patellofemoral pain syndrome, Pellegrini-Stieda syndrome, Pigmented villonodular synovitis, Piriformis syndrome, Plantar fasciitis, Polyarteritis nodosa, Polymyalgia rheumatica, Polymyositis, Popliteal cysts, Posterior tibial tendinitis, Pott's disease, Prepatellar bursitis, Prosthetic joint infection, Pseudoxanthoma elasticum, Psoriatic arthritis, Raynaud's phenomenon, Reactive arthritis/Reiter's syndrome, Reflex sympathetic dystrophy syndrome, Relapsing polychondritis, Retrocalcaneal bursitis, Rheumatic fever, Rheumatoid arthritis, Rheumatoid vasculitis, Rotator cuff tendinitis, Sacroiliitis, Salmonella osteomyelitis, Sarcoidosis, Saturnine gout, Scheuermann's osteochondritis, Scleroderma, Septic arthritis, Seronegative arthritis, Shigella arthritis, Shoulder-hand syndrome, Sickle cell arthropathy, Sjogren's syndrome, Slipped capital femoral epiphysis, Spinal stenosis, Spondylolysis, Staphylococcus arthritis, Stickler syndrome, Subacute cutaneous lupus, Sweet's syndrome, Sydenham's chorea, Syphilitic arthritis, Systemic lupus erythematosus (SLE), Takayasu's arteritis, Tarsal tunnel syndrome Tennis elbow, Tietse's syndrome, Transient osteoporosis, Traumatic arthritis, Trochanteric bursitis, Tuberculosis arthritis, Arthritis of Ulcerative colitis, Undifferentiated connective tissue syndrome (UCTS), Urticarial vasculitis, Viral arthritis, Wegener's granulomatosis, Whipple's disease, Wilson's disease and Yersinial arthritis. That's 171 types!
What are the different types of heart disease?
Coronary artery disease (CAD) is the most common type and is the leading cause of heart attacks. When you have CAD, your arteries become hard and narrow. Blood has a hard time getting to the heart, so the heart does not get all the blood it needs. CAD can lead to: Angina. Angina is chest pain or discomfort that happens when the heart does not get enough blood. Myocardial Infarction (MI) or Heart Attack Arrhythmia or Irregular Heart Rhythm Atrial Fibrillation Heart Valve Disease Congenital Heart Disease Cardiomyopathy (Heart Muscle Disease) Dilated Cardiomyopathy Hypertrophic Cardiomyopathy Restrictive Cardiomyopathy Cardiomegaly (Enlarged Heart) Pericarditis Pericardial Effusion Marfan Syndrome Heart Murmurs
What is the life expectancy of a patient with Marfan syndrome?
Recent advances in Marfan syndrome treatment have prolonged the life expectancy of patients considerably. Changes in how the syndrome is treated, including medication, surgical interventions, and monitoring for complications of the syndrome (eg, aneurysms), are all responsible for the increase in life expectancy. The prolongation in life expectancy can be seen by taking a look at statistics from 1972, in which the life expectancy was 32 years, and from 1996, where patients with Marfan syndrome had a life expectancy of 61 years.
Why do Marfan syndrome sufferers develop longer bones?
Marfan syndrome causes an increase in the length of the patient's bones, with decreased support from the ligaments that hold the bones together.
Why are eye conditions important in diagnosing cases of Marfan syndrome?
Although the visual problems that are related to Marfan syndrome are rarely life-threatening, they are important in that they may be the patient's first indication of the disorder.
What are the chances of getting marfan syndrome?
Marfan syndrome is found in 1 in every 5,000 - 10,000 births. If one of your parents has Marfan syndrome, you have a 50% chance of having Marfan syndrome.
What other inherited disease can be confused with Marfan syndrome?
The symptoms of Marfan syndrome in some patients resemble the symptoms of homocystinuria, which is an inherited disorder marked by extremely high levels of homocystine in the patient's blood and urine.
What are common external signs of Marfan syndrome?
The most common external signs associated with Marfan syndrome include excessively long arms and legs, with the patient's arm span being greater than his or her height.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
What does Marfan syndrome mean?
Marfan Syndrome is a medical problem with the Conective Tissue.
Is Marfan syndrome contagious?
Marfan's syndrome is not contagious. A person can only get it by inheriting it from a parent.
What treatment is recommended for Marfan syndrome sufferers?
The treatment and management of Marfan is tailored to the specific symptoms of each patient. Some patients find that the syndrome has little impact on their overall lifestyle; others have found their lives centered on the disorder.
Is Down Syndrome the same as Marfan Syndrome?
No. Down is caused by an extra chromosome while Marfan is due to a mutation in one or more genes.
How is the acetabulum impacted by Marfan syndrome?
The acetabulum is the socket of the hip joint. In patient's with Marfan, the acetabulum becomes deeper than normal during growth, for reasons that are not yet understood.
