| CASE REPORT |
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| Year : 2019 | Volume
: 6
| Issue : 2 | Page : 119-122 |
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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
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/cjhr.cjhr_104_18
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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.
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