Marfan syndrome

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Marfan syndrome


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USMLE® Step 1 questions

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High Yield Notes

6 pages


Marfan syndrome

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USMLE® Step 1 style questions USMLE

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A 25-year-old woman comes to an outpatient clinic to establish care. The patient has not seen a physician in several years but overall feels healthy except for blurry vision. She attributes this symptom to myopia caused by “spending too many hours in front of the laptop.” Past medical history is significant for pelvic inflammatory disease successfully treated with antibiotics. The patient was adopted as a young child and has never met her biological parents. Vitals are within normal limits. Slit-lamp examination is notable for bilateral upward lens subluxation. Physical examination reveals a patient at the 90th percentile for height and 50th percentile for weight. The patient also has long, tapering fingers and a prominent, protruding sternum. Oropharyngeal examination shows a high-arched palate with crowded teeth. This patient is most likely to develop which of the following complications?

External References

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Aortic aneurysm p. 308

Marfan syndrome p. 50, 306

Aortic dissection p. 309

Marfan syndrome p. 714

Marfan syndrome as cause p. 306

Aortic regurgitation

Marfan syndrome p. 306

Arachnodactyly p. 50

Marfan syndrome p. 714

Marfan syndrome

aortic aneurysms p. 728

aortic dissection and p. 309

cardiac defect association p. 306

cataracts p. 554

chromosome association p. 62

elastin and p. 50

heart murmur with p. 298

presentation p. 714

thoracic aortic aneurysms and p. 308


Content Reviewers

Marfan syndrome is a genetic disorder that results in defective connective tissue, which can affect a person’s skeleton, heart, blood vessels, eyes, and lungs.

Normally, the interstitial space of various body tissues is full of microfibrils - which are strong rope-like structures that provide tissue integrity and form connective tissue.

Each microfibril is made of cellulose as well as glycoproteins including the protein fibrillin. In some structures microfibrils form a scaffold for additional proteins like elastin.

Elastin fibers are highly cross-linked, and that gives them a rubber-band-like quality, which allows tissues to stretch and then spring back to their original shape.

Tissues that have elastin fibers are the arteries, skin, and lungs, and tissues that have microfibrils but no overlying layer of elastin are like tendons and the ciliary zonules that hold the eye lens in place.

These tissues are less stretchable, but still have considerable tensile strength.

In addition to being part of microfibrils, fibrillin also regulates tissue growth.

Fibrillin sequesters or removes transforming growth factor beta, or TGF-β, which stimulates tissue growth, so fibrillin therefore lowers how much TGF-β is available to stimulate growth.

Marfan syndrome is caused by mutations in a gene called FBN1, or fibrillin 1, on chromosome 15.

It’s autosomal dominant, which means that even if there’s a normal copy of the gene, a single mutated copy of the gene – in other words a heterozygous mutation – is sufficient to cause the disease.

The FBN1 gene encodes Fibrillin-1 protein, one of three fibrillin subtypes.

In Marfan syndrome, fibrillin-1 is either less abundant or it is dysfunctional. As a result, there are fewer functioning microfibrils in the extracellular matrix, and that means there’s less tissue integrity and elasticity.

Connective tissue is found throughout the body, so this can affect nearly every body system.

Additionally, TGF-β doesn’t get effectively sequestered, so TGF-β signaling is excessive in these tissues - meaning more growth.

The most obvious physical features of Marfan syndrome involve the skeleton.

The long bones grow excessively, so individuals are tall with long arms and legs – this is called a Marfanoid body habitus.


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