Different Cardiac Anomalies in Mother and Son with 4q-Syndrome
Joint Authors
Marcì, Marcello
Guarina, Angela
Castiglione, M. Cristina
Sanfilippo, Nicola
Source
Issue
Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2015-08-31
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
We report a female patient with asymptomatic cor triatriatum sinister, associated with 4q34.3 deletion.
Her child, carrying the same imbalance, suffers from tetralogy of Fallot.
To the best of our knowledge, this is the first reported case of cor triatriatum associated with deletion of the long arm of the chromosome 4; furthermore, the majority of patients with chromosome 4 long arm syndrome have de novo deletions and only few familial cases have been reported so far.
American Psychological Association (APA)
Marcì, Marcello& Guarina, Angela& Castiglione, M. Cristina& Sanfilippo, Nicola. 2015. Different Cardiac Anomalies in Mother and Son with 4q-Syndrome. Case Reports in Genetics،Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1058520
Modern Language Association (MLA)
Marcì, Marcello…[et al.]. Different Cardiac Anomalies in Mother and Son with 4q-Syndrome. Case Reports in Genetics No. 2015 (2015), pp.1-3.
https://search.emarefa.net/detail/BIM-1058520
American Medical Association (AMA)
Marcì, Marcello& Guarina, Angela& Castiglione, M. Cristina& Sanfilippo, Nicola. Different Cardiac Anomalies in Mother and Son with 4q-Syndrome. Case Reports in Genetics. 2015. Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1058520
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1058520