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Case Reports   |    
Cerebrotendinous Xanthomatosis: A Rare Cause of Bilateral Achilles Tendon Swelling and AtaxiaA Case Report
James W. Brodsky, MD1; Andrew D. Beischer, MD, FRACS2; Dip Anat2; Cara East, MD3; Elizabeth Soltero, CCRC3; G. Stephen Tint, PhD4; Gerald Salen, MD4; Julie Silverman, AB5
1 411 North Washington Avenue, Suite 7000, Dallas, TX 75246
2 32 Erin Street, Melbourne, INTL 3121, Australia
3 Clinical Cardiovascular Research Center, 3600 Gaston Avenue, Suite 1202, Dallas, TX 75246
4 Department of Medicine, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, 185 South Orange Avenue, Medical Science Building, I-506, Newark, NJ 07101-1709
5 12317 Montego Plaza, Dallas, TX 75230
The Journal of Bone & Joint Surgery.  2006; 88:1340-1344  doi:10.2106/JBJS.E.00872
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Extract

Cerebrotendinous xanthomatosis is a rare autosomal recessive lipid-storage disease caused by a mutation in the sterol 27-hydroxylase (CYP27) gene1,2. It is important that orthopaedic surgeons be aware of this condition because the initial presentation may be symmetric, painful enlargement and deformity of the Achilles tendons. Early diagnosis is the key to treatment because medical therapy is effective in halting progression of, although not reversing, the devastating neurological lesions of this condition.
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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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