Ruzicka Goerz Anton syndrome
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Ruzicka Goerz Anton syndrome is a rare genetic disease described by Ruzicka et al. in 1981. It is characterized by icthyosis (rough, scaly skin), deafness, intellectual disability, and skeletal anomalies.[1][2]
It is also known as "Ichthyosis deafness intellectual disability skeletal anomalies".[3]