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Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation

✍ Scribed by Hou-De Zhou; Yan-Hong Bu; Hui Xie; Yi-Qun Peng; Min Wan; Er-Yuan Liao

Book ID: 116320943
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 50 KB
Volume: 43
Category: Article
ISSN: 8756-3282
DOI: 10.1016/j.bone.2008.08.030

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## Abstract Progressive pseudorheumatoid dysplasia (PPD) is a rare autosomal recessive syndrome characterized by the presence of spondyloepiphyseal dysplasia associated with pain, stiffness, and swelling of multiple joints, osteoporosis, and the absence of destructive bone changes. The disorder is