home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 1026      Small font sizeDefault font sizeIncrease font size Print this page Email this page
Year : 2015  |  Volume : 10  |  Issue : 2  |  Page : 175-177

Rubinstein-Taybi syndrome with agenesis of corpus callosum

Department of Paediatrics, MKCG Medical College, Berhampur, Odisha, India

Correspondence Address:
Shubhankar Mishra
At/Po Sadanandapur, Basta, Balasore 756 029, Odisha
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/1817-1745.159207

Rights and Permissions

Rubinstein-Taybi syndrome (RSTS) is a rare genetic disorder with characteristic morphological anomaly. Our patient was a 4.5-year-old girl came with features like broad thumbs, downward slanting palpebral fissures and mental retardation. Systemic abnormalities such as repeated infection, seizure with developmental delay were also associated with it. She was having head banging behavior abnormal slurring speech, incoordination while transferring things from one hand to other. Galaxy of clinical pictures and magnetic resonance imaging report helped to clinch the diagnosis as a case of "RSTS with corpus callosal agenesis" which to the best of our knowledge has never been reported in past from India.


Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)

 Article Access Statistics
    PDF Downloaded102    
    Comments [Add]    
    Cited by others 2    

Recommend this journal