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Spondyloepimetaphyseal dysplasia, Genevieve type

MONDO:0012495

A rare primary bone dysplasia characterized by severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips.

Also known as: SEMD, Geneviève type, SEMDG, spondyloepimetaphyseal dysplasia, Camera-Genevieve type, spondyloepimetaphyseal dysplasia, Genevieve type, Nans deficiency, SEMD Genevieve type, SEMD, Genevieve type, spondyloepimetaphyseal dysplasia Genevieve type

0 clinical trials for this condition and its sub-types, 0 tagged with Spondyloepimetaphyseal dysplasia, Genevieve type itself.

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