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RGUHS Nat. J. Pub. Heal. Sci Vol: 14  Issue: 1 eISSN:  pISSN

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: 434, Downloads: 2
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CC BY NC 4.0 ICON
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.

<p>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.</p>
Keywords
mesomelic, hemivertebrae, foetal facies
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