Author/Authors :
Kumar K Jagadish نويسنده Department of Pediatrics, JSS Medical College, JSS University, Mysore , Nayana N نويسنده JSS Medical College, Mysore, India , Manjunath V G نويسنده JSS Medical College, Mysore, India , Shetty Chandrashekar نويسنده JSS Medical College, Mysore, India
Abstract :
Pseudoachondroplasia is a rare type of short-limbed skeletal
dysplasia. It is usually found as an autosomal dominant inheritable
disorder. Children are normal at birth and they present developmental
delay in walking by the age of 2, an abnormal waddling gait or
deformities of the lower limb. Diagnosis is based on characteristic
clinical and radiological findings. This study reports on a 6-year-old
boy with classical features of pseudoachondroplasia.