Marfan syndrome

Christopher G. Harris; Beth Croce; David H. Tian

doi:10.3978/j.issn.2225-319X.2014.07.09

Marfan syndrome

Christopher G. Harris, Beth Croce (Illustrator), David H. Tian (Editor)

Research output: Contribution to journal › Article › peer-review

Abstract

Marfan syndrome is a genetic disorder that affects connective tissue in the body. This disorder can be inherited from an affected parent or may occur through a spontaneous genetic mutation. Connective tissue is a necessary structural component in the body as it holds tissues and organs together and ensures normal growth and development. Since it is found throughout the body, many different organs can be affected by the disorder. These include the heart, blood vessels, eyes, lungs, bones, joints and skin. Some of these defects can lead to serious complications and may be life-threatening. Early diagnosis and treatment are necessary to prevent these complications and ensure a good quality of life for those affected.

Original language	English
Pages (from-to)	437
Number of pages	1
Journal	Annals of Cardiothoracic Surgery
Volume	3
Issue number	4
DOIs	https://doi.org/10.3978/j.issn.2225-319X.2014.07.09
Publication status	Published - Jul 2014

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10.3978/j.issn.2225-319X.2014.07.09

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title = "Marfan syndrome",

abstract = "Marfan syndrome is a genetic disorder that affects connective tissue in the body. This disorder can be inherited from an affected parent or may occur through a spontaneous genetic mutation. Connective tissue is a necessary structural component in the body as it holds tissues and organs together and ensures normal growth and development. Since it is found throughout the body, many different organs can be affected by the disorder. These include the heart, blood vessels, eyes, lungs, bones, joints and skin. Some of these defects can lead to serious complications and may be life-threatening. Early diagnosis and treatment are necessary to prevent these complications and ensure a good quality of life for those affected.",

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DO - 10.3978/j.issn.2225-319X.2014.07.09

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Marfan syndrome

Abstract

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