Marfan syndrome - Skin
FBN1 is found throughout the body, explaining the numerous manifestations of the syndrome. The most commonly affected organ systems are the cardiovascular, skeletal, and ocular systems. These organ systems are particularly susceptible because they contain an abundant amount of FBN1. Common manifestations include hyperextensible joints, lens dislocation, skeletal abnormalities, and aortic aneurysms.
Cutaneous manifestations are less common, but striae distensae occur in two-thirds of patients. Inguinal or incisional hernias are also more commonly seen in affected individuals. Elastosis perforans serpiginosa is a rare cutaneous feature.
Marfan syndrome affects approximately 1:5000–10000 individuals without predilection for age, sex, or ethnicity. Clinical features become more apparent with increasing age.
Pediatric Patient Considerations:
This condition is difficult to diagnose in children, as many features are age dependent.
For more information, see OMIM.
Q87.40 – Marfan's syndrome, unspecified
19346006 – Marfan syndrome
- MASS phenotype (mitral, aortic, skin, and skeletal) – Similar constellation of findings but does not fit diagnostic criteria for Marfan syndrome.
- Homocystinuria – Plasma homocysteine elevated, lens displaced downward.
- Loeys-Dietz aortic aneurysm syndrome – Similar systemic features but more severe aortic dissections, hypertelorism, broad or bifid uvula, and torturous arteries.
- Ehlers-Danlos syndrome – Also associated with EPS and hyperextensible skin and joints; may present with poor wound healing and bruises; cardiac abnormalities are less common.
- Cutis laxa – Hyperextensible skin that remains loose when stretched; associated with pulmonary emphysema, bladder diverticula, and pulmonary artery stenosis.