Journal of Pediatric Neurosciences
CASE REPORT
Year
: 2016  |  Volume : 11  |  Issue : 1  |  Page : 83--85

Warburg micro syndrome in siblings from India


Prabhjot Kaur Sekhon, R Premalatha, Sarala Sabapathy 
 Department of Pediatrics, Bangalore Medical College and Research Institute, Bengaluru, Karnataka, India

Correspondence Address:
Prabhjot Kaur Sekhon
Department of Pediatrics, Bangalore Medical College and Research Institute, Bowring and Lady Curzon Hospital, Lady Curzon Road, Tasker Town, Shivaji Nagar, Bengaluru - 560 001, Karnataka
India

Warburg syndrome is a rare disorder characterized by microcephaly, microcornea, congenital cataract, developmental delay, and hypogonadism. Here, we report two siblings from India who presented with developmental delay, microcornea, microphthalmia, and bilateral congenital cataracts, born to the third-degree consanguineously married couple. Both children had hypoplasia of corpus callosum. In this report, we aim to highlight and compare clinical features of these two cases with previously reported cases.


How to cite this article:
Sekhon PK, Premalatha R, Sabapathy S. Warburg micro syndrome in siblings from India.J Pediatr Neurosci 2016;11:83-85


How to cite this URL:
Sekhon PK, Premalatha R, Sabapathy S. Warburg micro syndrome in siblings from India. J Pediatr Neurosci [serial online] 2016 [cited 2022 May 24 ];11:83-85
Available from: https://www.pediatricneurosciences.com/article.asp?issn=1817-1745;year=2016;volume=11;issue=1;spage=83;epage=85;aulast=Sekhon;type=0