ABC Medical Center > FIBRILLIN MUTATION

FIBRILLIN MUTATION

Indications:

No special indications

What it's for:

Auxiliary in diagnosing: - Marfan syndrome associated with FBN1. -Autosomal dominant ectopia lentis. -Isolated ascending aortic aneurysm and dissection. -Isolated skeletal features of Marfan syndrome. -MASS phenotype (mitral valve prolapse, increased aortic diameter, striae, MFS skeletal features) -Shprintzen-Goldberg syndrome. -Autosomal dominant Weill-Marchesani syndrome.

Delivery time:

40 business days

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