Cardiac anomalies-heterotaxy syndrome

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Cardiac anomalies-heterotaxy syndrome is characterised by non-compaction of the ventricular myocardium bradycardia pulmonary valve stenosis and secundum atrial septal defect. Laterality sequence anomalies are also present. So far the syndrome has been described in nine members from three generations of the same family. Transmission is autosomal dominant and linkage to chromosome 6p24.3-21.2 was reported.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version June 2024

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