Holt oram syndrome

0Citations
Citations of this article
13Readers
Mendeley users who have this article in their library.

Abstract

Holt Oram Syndrome, an autosomal dominant disorder is constellation of congenital heart diseases and skeletal abnormalities. Amongst the congenital heart defects ostium secundum type of atrial septal defect is most common. Electrocardiographic abnormalities include heart blocks and AV conduction defects up to variable extent. In addition to cardiac abnormalities skeletal abnormalities such as radial dysplasia or hypoplasia and other upper limb abnormalities have been reported. We are presenting a case 25 years old lady with Holt Oram syndrome presenting with cardiac failure.

Cite

CITATION STYLE

APA

Patel, S. K., Kumar, A., Yadav, M., Bohania, N., & Kumar, A. (2015). Holt oram syndrome. Research Journal of Pharmaceutical, Biological and Chemical Sciences, 6(4), 596–598. https://doi.org/10.5958/2349-2996.2017.00026.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free