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Marfan Syndrome
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Published on Nov 18, 2015
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PRESENTATION OUTLINE
1.
MARFAN'S SYNDROME
2.
WHO DISCOVERED IT?
ANTIONE B. MARFAN
3.
CURRENT STATUS
Marfan syndrome is a disease of connective tissues that is inherited
Currently there is no treatment for Marfans syndrome
There is medicine to help through pain though
Photo by
takacsi75
4.
SYMPTOMS
Unusually tall
Flat feet
Abnormally skinny
Very curved spine
5.
WHATS AFFECTED?
Affects the body's connective tissue
Connective tissue plays a role in your growth
Affects bones and skin
6.
HOW DO YOU GET THE SYNDROME?
Caused by a defect, or mutation, in the gene structure of fibrillin.
It is not sex- linked
Marfan syndrome can be inherited:
he child of a person who has Marfan syndrome has a 50 percent chance of inheriting the disease
7.
DIAGNOSED
You are born with the disease
But may not be diagnosed until later in life
Diagnosed by connective tissue disorder
8.
SOURCES
"What Is Marfan Syndrome?" - NHLBI, NIH. NIH, 5 Feb. 2012. Web. 11 Dec. 2013.
http://www.marfan.org/about/body-systems
MedicineNet." MedicineNet. Medicine Net, 8 June 2013. Web. 11 Dec. 2013.
http://www.medicinenet.com/marfan_syndrome/article.htm
"Genetics of Marfan Syndrome Treatment & Management." Genetics of Marfan Syndrome Treatment & Management. Medscape, 9 May 2013. Web. 13 Dec. 2013.
http://www.niams.nih.gov/Health_Info/Marfan_Syndrome/marfan_syndrome_ff.asp
http://www.marfan-association.org.uk/id13.html#faq0
9.
THE END
Tristan Kalina
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