Marfan Syndrome

From WikiMD.org
Jump to navigation Jump to search
Marfan Syndrome
TermMarfan Syndrome
Short definitionMarfan Syndrome - (pronounced) (MAR fan SIN-Drome) A genetic disorder affecting the connective tissues in many organs and tissues of the body, particularly the heart, eyes, bones, joints, and blood vessels, including the aorta. People with Marfan syndrome are often tall and thin, have very long arms, legs, fingers, and toes, and have heart and vision problems. 
TypeCancer terms
SpecialtyOncology
LanguageEnglish
SourceNCI
Comments


Marfan Syndrome - (pronounced) (MAR fan SIN-Drome) A genetic disorder affecting the connective tissues in many organs and tissues of the body, particularly the heart, eyes, bones, joints, and blood vessels, including the aorta. People with Marfan syndrome are often tall and thin, have very long arms, legs, fingers, and toes, and have heart and vision problems. Other common signs and symptoms include a long and narrow face, crowded teeth, a curved spine, loose joints, stretch marks in the skin, and breast abnormalities. Marfan syndrome can be inherited (passed from parent to child) and is caused by a mutation (change) in a gene called FBN1

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski