Robinow Syndrome

Muralidhar L Kulkarni; Sidramayya SS; Vivekanand VV; Akhil M Kulkarni; Srikanth CH; Rupinder Kaurnbsp

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RGUHS Nat. J. Pub. Heal. Sci Vol: 14 Issue: 4 eISSN: pISSN

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Case Report

Robinow Syndrome

Muralidhar L. Kulkarni ¹, Sidramayya S.S ², Vivekanand V.V ², Akhil M Kulkarni ³, Srikanth C.H ², Rupinder Kaur ²

¹Professor and Head, ²Resident, Department of Paediatrics,³ Assistant Professor, Department of Radiodiagnosis, JJM Medical College, Davangere

Year: 2013, Volume: 3, Issue: 1, Page no. 56-58,

Views: 599, Downloads: 4

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0.

Abstract

Robinow syndrome is a rare genetic disorder of mesomelic dwarfism with characteristic dysmorphic features. It is a syndrome of mesomelic limb shortening, hemivertebrae , genital hypoplasia and characteristic foetal facies.

Keywords

mesomelic, hemivertebrae, foetal facies

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