CHRISMED Journal of Health and Research

CASE REPORT
Year
: 2019  |  Volume : 6  |  Issue : 2  |  Page : 119--122

Holt–Oram syndrome – Case series of two reports


Mohd Ilyas, Arif Ahmad Wani, Zubair Ahmad, Mir Junaid Ahmad Kazimi, Naseer A Choh 
 Department of Radiodiagnosis, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India

Correspondence Address:
Mohd Ilyas
Department of Radiodiagnosis, Sher-I-Kashmir Institute of Medical Sciences, Srinagar - 190 011, Jammu and Kashmir
India

Holt–Oram syndrome is a rare genetic autosomal dominant disorder which affects the upper limbs and heart. It is also known as “heart–hand” syndrome or “atriodigital dysplasia.” The present article describes the clinical and radiological images of the features of Holt–Oram syndrome in two patients.


How to cite this article:
Ilyas M, Wani AA, Ahmad Z, Ahmad Kazimi MJ, Choh NA. Holt–Oram syndrome – Case series of two reports.CHRISMED J Health Res 2019;6:119-122


How to cite this URL:
Ilyas M, Wani AA, Ahmad Z, Ahmad Kazimi MJ, Choh NA. Holt–Oram syndrome – Case series of two reports. CHRISMED J Health Res [serial online] 2019 [cited 2021 Apr 18 ];6:119-122
Available from: https://www.cjhr.org/article.asp?issn=2348-3334;year=2019;volume=6;issue=2;spage=119;epage=122;aulast=Ilyas;type=0