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Spondyloenchondromatosis: Syndromic identity and evolution of the phenotype

โœ Scribed by Zack, P. ;Beighton, P.

Book ID
102703530
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
504 KB
Volume
55
Category
Article
ISSN
0148-7299

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โœฆ Synopsis

W e present case details and depict the phenotypic manifestations of a dwarfing skeletal dysplasia in an adolescent boy who was first seen in early childhood. His initial clinical and radiological findings resembled those of pseudoachondroplasia but these subsequently metamorphosed to an appearance which was diagnostic of spondyloenchondromatosis. It is uncertain whether this latter condition is a homogeneous entity or a group of heterogeneous disorders. Pedigree data were consistent with autosomal recessive inheritance.

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