| Literature DB >> 21863289 |
Stefan F Nemec1, Daniel H Cohn, Deborah Krakow, Vincent A Funari, David L Rimoin, Ralph S Lachman.
Abstract
The spondylo and spondylometaphyseal dysplasias (SMDs) are characterized by vertebral changes and metaphyseal abnormalities of the tubular bones, which produce a phenotypic spectrum of disorders from the mild autosomal-dominant brachyolmia to SMD Kozlowski to autosomal-dominant metatropic dysplasia. Investigations have recently drawn on the similar radiographic features of those conditions to define a new family of skeletal dysplasias caused by mutations in the transient receptor potential cation channel vanilloid 4 (TRPV4). This review demonstrates the significance of radiography in the discovery of a new bone dysplasia family due to mutations in a single gene.Entities:
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Year: 2011 PMID: 21863289 DOI: 10.1007/s00247-011-2229-6
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449