Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome

J Pediatr. 2020 Mar:218:263-264. doi: 10.1016/j.jpeds.2019.10.050. Epub 2019 Dec 13.

Authors

M Cristina Digilio¹, Giulio Calcagni¹, Alessandro De Luca², Valentina Guida², Bruno Marino³

Affiliations

¹ Medical Genetics and Pediatric Cardiology, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
² Molecular Genetics Unit, Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Foggia, Italy.
³ Department of Pediatrics, Sapienza University, Rome, Italy.

PMID: 31843215
DOI: 10.1016/j.jpeds.2019.10.050

No abstract available

Publication types

Letter
Comment

MeSH terms

Bardet-Biedl Syndrome*
Heart Septal Defects*
Heterotaxy Syndrome*
Humans
Situs Inversus*

Supplementary concepts

Atrioventricular Septal Defect