CHRISMED Journal of Health and Research (Jan 2019)

Holt–Oram syndrome – Case series of two reports

  • Mohd Ilyas,
  • Arif Ahmad Wani,
  • Zubair Ahmad,
  • Mir Junaid Ahmad Kazimi,
  • Naseer A Choh

DOI
https://doi.org/10.4103/cjhr.cjhr_104_18
Journal volume & issue
Vol. 6, no. 2
pp. 119 – 122

Abstract

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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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