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.
CITATION STYLE
Thong, M. K., Scherer, G., Kozlowski, K., Haan, E., & Morris, L. (2000). Acampomelic campomelic dysplasia with SOX9 mutation. Genetics in Medicine, 2(1), 88. https://doi.org/10.1097/00125817-200001000-00136
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