hrp0092p3-36 | Bone, Growth Plate and Mineral Metabolism | ESPE2019

A Case of Robinow Syndrome

Anil Korkmaz Huseyin , Sen Askin

Introduction: Robinow syndrome is a rare autosomal recessive and autosomal dominant disorder affecting the whole skeletal system. Autosomal recessive robinow syndrome is characterized by shortness of the long bones and vertebra anomalies. Less than 200 cases of autosomal recessive robinow syndrome have been reported in the literature.Case: The newborn was referred to pediatric endocrine clinic for disorder of penis devel...