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Marfan's syndrome overview

Introduction

Editors-In-Chief: William James Gibson, C. Michael Gibson, M.S., M.D.

Overview

Overview

Marfan syndrome (or Marfan’s syndrome) is a connective tissue disorder most often caused by defects in the Fibrillin-1 gene (FBN1). Patients with Marfan’s syndrome are at significant risk of skeletal, cardiovascular and ocular complications. People with Marfan’s are typically tall, with long limbs and long thin fingers.

References

References

Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [1] ; Cassandra Abueg, M.P.H. [2]