Holt–Oram syndrome – Case series of two reports
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....
Main Authors: | Mohd Ilyas, Arif Ahmad Wani, Zubair Ahmad, Mir Junaid Ahmad Kazimi, Naseer A Choh |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2019-01-01
|
Series: | CHRISMED Journal of Health and Research |
Subjects: | |
Online Access: | http://www.cjhr.org/article.asp?issn=2348-3334;year=2019;volume=6;issue=2;spage=119;epage=122;aulast=Ilyas |
Similar Items
-
Holt-Oram Syndrome: A Rare Variant
by: Binoy Shankar, et al.
Published: (2017-07-01) -
Genetics of the Holt-Oram syndrome.
by: Chan, Lily Wai-Li
Published: (1971) -
Holt-Oram syndrome: Anesthetic challenges and safe outcome
by: Meenal Rana, et al.
Published: (2017-01-01) -
Diagnosis of absent right superior vena cava with intraoperative transesophageal echocardiography in a child with Holt-Oram syndrome: Anesthetic and perfusion implications
by: Satyajeet Misra, et al.
Published: (2021-01-01) -
A genetic Assay of Three Patients in the Same Family with Holt-Oram Syndrome; a Case Report
by: Reza Ebrahimzadeh-Vesal, et al.
Published: (2013-10-01)