| Literature DB >> 10951468 |
M K Thong1, G Scherer, K Kozlowski, E Haan, L Morris.
Abstract
Acampomelic campomelic dysplasia is a rare clinical variant of the more commonly encountered campomelic dysplasia (CMD1), characterized by absence of long bone curvature (acampomelia). We present a patient with acampomelic CMD1 with a de novo SOX9 missense mutation and report his clinical course to age one year, thereby contributing to genotype-phenotype correlation in CMD1. 2000. Copyright 2000 Wiley-Liss, Inc.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10951468
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299