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Pycnodysostosis: A Review
STANLEY M. ELMORE
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From the Department of Orthopaedic Surgery, Vanderbilt University School of Medicine, Nashville, Tennessee
1967 by The Journal of Bone and Joint Surgery, Incorporated
The Journal of Bone & Joint Surgery.  1967; 49:153-162 
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Abstract

The characteristics of pycnodysostosis, a new syndrome named in 1962, are reviewed in thirty-three cases taken from the literature. Pycnodysostosis is a genetic disease of bone characterized by short stature, skull dysplasia, flattened mandibular angle, dysplasia of the clavicles and terminal phalanges, increased bone density, and normal laboratory studies. Pycnodysostosis must be distinguished from cleidocranial dysostosis, osteopetrosis, progressive diaphyseal dysplasia, and idiopathic nonfamilial acro-osteolysis.

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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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