CC BY 4.0 · Indian J Plast Surg 2008; 41(01): 076-078
DOI: 10.4103/0970-0358.41118
Case Report

Radial, renal and craniofacial anomalies: Baller-Gerold syndrome

Jyotsna Murthy
1   Department of Plastic Surgery, Director of Cleft and Craniofacial Center, Consultant Pediatric Urologist, Porur, Chennai, Tamil Nadu, India
,
Ramesh Babu
1   Department of Plastic Surgery, Director of Cleft and Craniofacial Center, Consultant Pediatric Urologist, Porur, Chennai, Tamil Nadu, India
,
Padmasani Venkat Ramanan
2   Department of Plastic Surgery, Director of Cleft and Craniofacial Center, Department of Pediatrics, Sri Ramachandra Medical College and Research Institute, Porur, Chennai, Tamil Nadu, India
› Author Affiliations
Source of Support: Nil.

Abstract

The Baller-Gerold syndrome is a rare syndrome with very few cases published in literature. Craniosynostosis and radial aplasia are striking features, easy to diagnose. However, there are many differential diagnoses. Often, the question raised is whether the Baller-Gerald syndrome is a distinct entity. We report a patient with findings of craniosynostosis and radial aplasia consistent with the diagnosis of the Baller-Gerold syndrome. Genotypic heterogeneity could possibly underlie the phenotypic variability exhibited by these cases.



Publication History

Article published online:
23 January 2025

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