Holt-Oram Syndrome: A Rare Variant

Holt-Oram Syndrome: A Rare Variant

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are b...

Full description

Bibliographic Details
Main Authors: Binoy Shankar, Euden Bhutia, Dinesh Kumar, Sunil Kishore, Shakti Pad Das
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2017-07-01
Series:Iranian Journal of Medical Sciences
Subjects:
Holt-Oram syndrome
Congenital heart disease
Tricuspid atresia
Online Access:http://ijms.sums.ac.ir/index.php/IJMS/article/view/2649

Similar Items

Similar Items