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14 Possible Causes for Arrhythmias Detected Prenatally, Atrial Septal Defect

  • Asplenia Syndrome

    […] and ventricular septal defects.[] Electrocardiogram (ECG): This is useful in the detection of arrhythmias and other abnormalities in cardiac function Echocardiogram: This is a non-invasive imaging technique[] The most common congenital heart defects were atrial septal defects, common atrioventricular canals and conotruncal anomalies.[]

  • Levocardia

    抄録 A case of levocardia with anomalous venous drainage of all right pulmonary veins to the right atrium, a sinus venosus type atrial septal defect, an anomalous inferior vena[] Postnatally, intestinal malrotation with no evidence of intestinal obstruction or asplenia was detected. Neither of the cases had reported cardiac arrhythmias.[] defect - Atrial septal defect ( Lutembacher's syndrome ) - Atrioventricular septal defect ( Ostium primum ) - Tetralogy of Fallot - Eisenmenger's syndrome Right: pulmonary[]

  • Ductus Arteriosus Aneurysm

    The atrial septal defect was closed in a separate procedure.[] Am J Cardiol 2000, 85: 1159-1161. 10.1016/S0002-9149(00)00718-9 View Article PubMed Google Scholar Chobot V, Hornberger L, Hagen-Ansert S, Sahn D: Prenatal detection of restrictive[] NIH: National Heart, Lung, and Blood Institute Atrial septal defect (Medical Encyclopedia) Bicuspid aortic valve (Medical Encyclopedia) Congenital heart defect corrective[]

  • Familial Cutaneous Collagenoma

    Fibrillation Right Ventricular Cardiomyopathy Atrial Septal Defect Cardiomyopathy Angina pectoris Skin Nodule Skin benign neoplasm Collagen Diseases Neoplastic diseases Rare[] These occur in approximately 50-70% of individuals with TSC, and are most frequently detected prenatally or in the neonatal period.[] septal defect An opening in the wall separating the top two chambers of the heart Hole in heart wall separating two upper heart chambers [ more ] 0001631 Cardiomyopathy Disease[]

  • Incessant Infant Ventricular Tachycardia

    septal defect.[] Supraventricular Tachycardia SVT is the most common serious arrhythmia detected prenatally. It accounts for about 6% of referrals, as shown in Table 2.[] Atrial Septal Defect In Children Autoimmune Diseases In Children Kawasaki Disease In Children How can we improve it? This article contains incorrect information.[]

  • Tachyarrhythmia

    septal defect in adults.[] Overall, these serious tachyarrhythmias comprise less than 10% of arrhythmias detected prenatally.[] Less common cardiac causes include cardiomyopathy, pericarditis, myocarditis, atrial septal defect, congenital heart disease and atrial myxoma.[]

  • Familial Atrial Fibrillation

    Familial, 9; ATFB9 OMIM:108800 Atrial Septal Defect 1; ASD1 OMIM:607941 Atrial Septal Defect 2; ASD2 OMIM:614089 Atrial Septal Defect 3; ASD3 OMIM:611363 Atrial Septal Defect[] , congenital, and other congenital anomalies, Atrial septal defect 9, atrioventricular septal defect 5, Persistent truncus arteriosus, Tetralogy of Fallot AD 16 82 HCN4 Sick[] 4; ASD4 OMIM:612794 Atrial Septal Defect 5; ASD5 OMIM:613087 Atrial Septal Defect 6; ASD6 OMIM:108900 Atrial Septal Defect 7 with or without Atrioventricular Conduction Defects[]

  • Renal Teratoma

    Defects of heart septum Atrial septal defects Ventricular septal defects AV septal defects Anomalies of the great arteries Transposition of the great arteries Truncus arteriosus[] Although cardiac tumors can easily be detected by prenatal US at as early as 20 weeks of gestation, diagnosis requires that they are of sufficient size.[] Congenital malformations of penis and scrotum Smith-Lemli-Opitz syndrome (SLOS) Congenital tumors Sacrococcygeal teratoma Congenital cardiac rhabdomyoma Congenital heart defects[]

  • Cross Syndrome

    septal defect Skeletal muscle atrophy Anemia Poikiloderma Flat nasal alae Preeclampsia Neoplasm of the eye Ankyloblepharon Conjunctival telangiectasia Giant melanosomes in[] Rhabdomyomas are found in 50% of people with TSC and are often detected on prenatal ultrasound.[] Arthralgia Telangiectasia of the skin Freckling Lymphadenopathy Visual impairment Ranula Difficulty walking Reduced visual acuity Recurrent infections Cerebellar atrophy Atrial[]

  • Northern Epilepsy

    septal defect, coronary sinus type Atrial septal defect, ostium secundum type Ataxia - Genetic diagnosis - Unknown Ataxia - oculomotor apraxia type 1 Ataxia - Other Ataxia[] These occur in approximately 50-70% of individuals with TSC, and are most frequently detected prenatally or in the neonatal period.[] septal defect sinus venosus Limb-girdle muscular dystrophy type 1A Neural tube defects Dubin-Johnson syndrome Ring chromosome 15 Schaefer Stein Oshman syndrome Mesomelic[]

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