Answer: Marfan syndrome. Clinical features of Marfan syndrome include: (A) arachnodactyly, (B) Walker-Murdoch “wrist” sign, (C) Steinberg “thumb” sign, (D) pectus deformity of excavatum, (E) pectus deformity of pectus carinatum, (F) pes planus with hindfoot deformity, (G) high arched, narrow palate, (H) ectopic lentis, (I) striae of skin, (J) significant dilation of the aortic root via 3-dimensional reconstruction from magnetic resonance, (K) aortic root dilation with angiography, and (L) dural ectasia.
From: Kline MW. Rudolph's Pediatrics, 23e; 2017 Available at: http://accesspediatrics.mhmedical.com/ViewLarge.aspx?figid=175123392&gbos Accessed: February 13, 2018
Create a Free MyAccess Profile
AccessMedicine Network is the place to keep up on new releases for the Access products, get short form didactic content, read up on practice impacting highlights, and watch video featuring authors of your favorite books in medicine. Create a MyAccess profile and follow our contributors to stay informed via email updates.