What can cause ventricular septal defect?

Down syndrome Turner syndrome Tetralogy of Fallot 1p36 deletion syndrome Di George's syndrome Wolf-Hirschhorn syndrome Ivemark syndrome Alagille syndrome Holt-Oram syndrome Double outlet right ventricle Asymmetric crying facies Hydrolethalus syndrome Aase-Smith syndrome Oculofaciocardiodental syndrome Congenitally corrected transposition of great arteries Microphthalmia-dermal aplasia-sclerocornea syndrome Osteoporosis-pseudoglioma syndrome Seemanova-Lesny syndrome Chromosome 15q deletion syndrome Endocardial cushion defect Maladie de Roger Velocardiofacial syndrome Myocardial infarction.

Asymmetric crying facies Cayler cardiofacial syndrome (unilateral facial weakness which may be associated with heart defects) wikipedia Hydrolethalus syndrome Hydrolethalus syndrome, the rare genetic disorder that causes improper fetal development, resulting in birth defects and often stillbirth wikipedia Aase-Smith syndrome Aase-Smith syndrome, characterized by the presence of three phlangeal bones, instead of the normal two Oculofaciocardiodental syndrome Oculofaciocardiodental syndrome, the cause and medical concept with DiseasesDB code "34589" Congenitally corrected transposition of great arteries Congenitally corrected transposition of great arteries, the cause and medical concept with DiseasesDB code "34519" Microphthalmia-dermal aplasia-sclerocornea syndrome Microphthalmia-dermal aplasia-sclerocornea syndrome (linear areas of erythematous skin dysplasia involving the chin, neck, and head, occurring in association with microphthalmia, corneal opacities, and orbital cysts) Osteoporosis-pseudoglioma syndrome Osteoporosis-pseudoglioma syndrome (a rare syndrome characterized by generalized osteoporosis, pseudoglioma, and blindness usually due to retinal detachment) Seemanova-Lesny syndrome Seemanova-Lesny syndrome (microcephaly, microphthalmia, cataract, mental deficiency, spasticity hypogenitalism, and growth retardation are the principal clinical features) Chromosome 15q deletion syndrome Chromosome 15q deletion syndrome (deletion of the long arm of chromosome 15 usually associated with variable phenotype) Endocardial cushion defect Endocardial cushion defect (a spectrum of septal defects involving the atrial septum; ventricular septum; and the atrioventricular valves (tricuspid valve; bicuspid valve)) Maladie de Roger Maladie de Roger, the cause and medical concept with DiseasesDB code "30773" Velocardiofacial syndrome Velocardiofacial syndrome the medical condition Myocardial infarction Myocardial infarction (necrosis of the myocardium caused by an obstruction of the blood supply to the heart (coronary circulation)).

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