Marfan syndrome
A genetic syndrome inherited as an autosomal dominant trait. It is caused by mutations in the FBN1 gene. It is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.
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An informative case of Marian syndrome in a 6 year old boy. Marfan syndrome is a genetic condition that affects connective tissues. It can impact different parts of the human body, including the heart, blood vessels, lungs, skin, bones, joi...
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The most common cardiac lesions is dilatation of the aortic ring,sinuses of valsalva,and ascending aorta.the dilatation leads to progressive aortic regurgitation and may be complicated by acute aortic dissection.the risk of dissection is ma...
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Nice picture. Wonderful surgery .Thanks for sharing
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Recent Cases of Marfan syndrome
Browse recently discussed Marfan syndrome cases by specialistsTop Cases of Marfan syndrome
Selected by editors, top cases are known for unique problem or best solutionTop Marfan syndrome Doctors on Curofy
Top doctors who continously share their opinions on Marfan syndromeEye Care & Research Centre, Kolkata for About 25 Years
Consultant
Eye Care & Research Centre, Kolkata
MS, DO

Amritsar Eye Hospital
Director
G M C Amritsar
M S ophthalmology

National Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics

BMC HOSPITALS
MEDICAL OFFICER I/C.
College of General Practice
c gp.

Self Employed. Now Doing My Practice
Pediatric Consultant
MKCG MCH
MBBS and MD (pediatrics)

1824 Views
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