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 |
|
|
|
