Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata
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DOI: 10.1007/s00247-018-4098-8
Abstract: BackgroundChondrodysplasia punctata is a skeletal dysplasia caused by a diverse spectrum of etiologies, with outcomes ranging from antenatal demise to a normal life span. Prenatal detection can be challenging.ObjectiveTo review a series of cases of… read more here.
Keywords: phenotype; prenatal mri; chondrodysplasia punctata; binder phenotype ... See more keywords