Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan

Background: Leri-Weill dyschondrosteosis (LWD) is a pseudoautosomal form of skeletal dysplasia, characterized by abnormal craniofacial phenotype, short stature, and mesomelia of the upper and lower limbs.Methods: We describe two female patients with LWD.Their prime clinical complaints were severe bouts of migraine and antalgic gait.Results: Interes

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