Marfan syndrome is a disorder of connective tissue which causes
skeletal defects typically recognized in a tall, lanky person. A
person with Marfan syndrome may exhibit long limbs and spider-like
fingers, chest abnormalities, curvature of the spine and a
particular set of facial features including a highly arched palate,
and crowded teeth. The most significant of the defects in the
syndrome are cardiovascular abnormalities, which may include
enlargement (dilatation) of the base of the aorta. Since Marfan
syndrome is usually an inherited disorder, prospective parents with
a family history of Marfan syndrome should get genetic counseling.
Review Date: 05/10/2010
Reviewed By: Chad Haldeman-Englert, MD, Wake Forest University School of
Medicine, Department of Pediatrics, Section on Medical Genetics,
Winston-Salem, NC. Review provided by VeriMed Healthcare Network.
Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M.,
Inc.
A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org)