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Essay on Marfan Syndrome 2085 Words9 Pages Marfan syndrome is a primarily AN autosomal dominant disorderliness that affects 1 in 5000 citizenry worldwide. Marfan syndrome is connective tissue paper disorder that results in a chromosomal mutation in the FibrillinFibrillin is a glycoprotein, which is all important for the organisation of elastic fibers found in conjunctive tissue. Fibrillin is secreted into the extracellular matrix aside fibroblasts and becomes incorporated into the insoluble microfibrils, which appear to bring home the bacon a scaffold for deposition of elastin. 1 gene.
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Marfan syndrome is a heritable disease of the connective tissues that affect many organs such as the eyes, lungs, skeleton, heart, and blood vessels.
Echocardiogram marfan syndrome
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Marfan syndrome is letter a genetic disorder that affects the conjunctive tissue.
Marfan syndrome is a common heritable disorder of the connective tissue.
Marfan syndrome caused by letter a recurrent de novo missense mutation fashionable the fibrillin gene.
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While marfan syndrome is the most average type of fibrillinopathy, not all mutations in the fbn1 gene cause this syndrome.
Inheritance pattern of marfan syndrome
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Cardinal unaffected parents wealthy person a 1 fashionable 10,000 chance of having a baby with marfan syndrome.
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Marfan syndrome is caused away a mutation stylish the gene that regulates the body's production of fibrilliin-1.
Some complications of marfan syndrome can glucinium treated or prevented, including heart disease, bone.
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In that location are a turn of conditions that can result stylish kyphosis, including osteoporosis, disc degeneration, nascence defects, cancer and cancer treatments, and syndromes such every bit prader-willi disease operating theatre marfan syndrome.
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Besides perhaps having heart problems, citizenry with the marfan syndrome are frequently tall and cobwebby.
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Marfan syndrome is A disease causing personal effects to the affectionateness, blood vessels, eyes, lungs, bones and joints.
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Marfan syndrome introduction: the marfan syndrome is letter a disorder that is an inherited from the parents of a person.
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Even among members of the same family, the signs and symptoms of marfan syndrome vary widely — both in their features and fashionable their severity.
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Marfan syndrome essay marfan syndrome is a multisystem disorder resulting with clinical manifestations typically involving the bony, ocular, and vessel systems.
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The disease is letter a fibrinllinopathy that results from defective deduction of fibrillin 1.
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Almost research on mfs has dealt with younger age groups, because of the earlier average eld of death.
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Marfan syndrome rear end be challenging for doctors to name because many conjunctive tissue disorders wealthy person similar signs and essays about yourself for college symptoms.
Marfan syndrome is letter a connective tissue disorderliness, so affects many another structures, including the skeleton, lungs, eyes, heart and bloodline vessels.
2 the grandness of the copulative tissues support and determine the body's elasticity of the body's organs, maraca and.
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It's saved in both genders, and all ethnical groups.
Marfan syndrome is a heritable disorderliness of the conjunctive tissue with Associate in Nursing estimated prevalence of 1 in 5000 individuals and none predilection for either sex.
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About 1 person fashionable 5,000 to 10,000 is born with marfan syndrome.
What does Marfan syndrome do to your connective tissue?
This elastic fibrous tissue can also get sick and defective, some people might suffer from a disease known as Marfan Syndrome which is a very unique ‘’genetic hereditary disorder affecting fibers of the connective tissue inside body. ’’ (Mayo Foundation For Medical Education and Research, 2018).
Is there a cure or cure for Marfan syndrome?
‘’More than half the people who suffer from Marfan Syndrome will have a lens dislocation; this is characterized by the focusing lens in the eye moving out of place because its supporting structure has weakened. There is no cure and the connective tissues that got broken will not heal or reattach.
How often does Marfan syndrome occur with no family history?
Surprisingly, this genetic mutation can even occur with no family history present; when this occurs it is referred as a spontaneous mutation. According to The Marfan Foundation, about 1 in 5,000 people have Marfan Syndrome and its a 50% chance that the gene will pass along each time the patient decides to become a parent.
Last Update: Oct 2021
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Dorlean
26.10.2021 02:23
The disorder is primarily a connective tissue paper problem that affects a large quantity of organs, the skeleton, lungs, eyes, heart and stemma vessels.
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Lekia
27.10.2021 08:47
The condition most usually affects elderly women, though it derriere appear in citizenry of any age.
Marfan syndrome most usually affects the warmheartedness, eyes, blood vessels and skeleton.
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23.10.2021 10:50
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20.10.2021 07:54
Marfan's patients have to undergo multiple and extensive surgeries.
Marfan syndrome have you e'er thought about the disease that butt be passed downfield by your parents?
Dorr
26.10.2021 05:53
The marfan syndrome is inherited and affects many parts of the body.
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21.10.2021 11:15
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This picture illustrates Echocardiogram marfan syndrome.
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