Atrial septal defect type II and upper limb malformation in 40-year-old male as a manifestation of Holt-Oram syndrome

Cardiol J. 2019;26(3):302-303. doi: 10.5603/CJ.2019.0062.

Authors

Ewa Szymczyk¹, Paulina Wejner-Mik², Piotr Lipiec², Błażej Michalski², Jarosław D Kasprzak²

Affiliations

¹ Department of Cardiology, Medical University of Lodz, Poland. eszymczyk@ptkardio.pl.
² Department of Cardiology, Medical University of Lodz, Poland.

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / diagnosis*
Abnormalities, Multiple / genetics
Abnormalities, Multiple / therapy
Adult
Cardiac Catheterization / instrumentation
Echocardiography, Doppler, Color*
Echocardiography, Three-Dimensional*
Echocardiography, Transesophageal*
Heart Defects, Congenital / diagnosis*
Heart Defects, Congenital / genetics
Heart Defects, Congenital / therapy
Heart Septal Defects, Atrial / diagnosis*
Heart Septal Defects, Atrial / genetics
Heart Septal Defects, Atrial / therapy
Humans
Lower Extremity Deformities, Congenital / diagnosis*
Lower Extremity Deformities, Congenital / genetics
Lower Extremity Deformities, Congenital / therapy
Male
Predictive Value of Tests
Septal Occluder Device
Treatment Outcome
Upper Extremity Deformities, Congenital / diagnosis*
Upper Extremity Deformities, Congenital / genetics
Upper Extremity Deformities, Congenital / therapy

Supplementary concepts

Holt-Oram syndrome