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Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia

✍ Scribed by Hua Yue; Zhen-Lin Zhang; Jin-Wei He


Book ID
116321093
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
562 KB
Volume
44
Category
Article
ISSN
8756-3282

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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