Dextrocardia

Orpha code: 1666OMIM code:

Definicja

A rare, congenital, non-syndromic, developmental defect during embryogenesis characterized by positioning of the heart in the right hemithorax, with the base and apex of the heart pointing caudally and to the right, due to abnormalities of embryologic origin that are intrinsic to the heart itself. Situs inversus or situs solitus may be associated, with extracardiac visceral transposition anomalies usually present in the former case and additional cardiac defects (e.g. septal defects, transposition of the great arteries, double-outlet right ventricle, anomalous pulmonary venous return, tetralogy of Fallot) frequently observed in both cases.

Disease data
Klasyfikacja

Morphological anomaly

Kod ORPHA
1666
Kod OMIM
-
Kod ICD10
Q24.0
Kod ICD11
LA80.1

No additional description.

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