P20.02: Giant cardiac aneurism: an anomaly with difficult prenatal counselling
نویسندگان
چکیده
منابع مشابه
Digeorge syndrome presenting with uncommon cardiac anomaly and hepatomegaly
Digeorge syndrome is caused by microdeletion of a large region of chromosome 22q11.2 lead to the abnormal development of the third and fourth pharyngeal pouches. This syndrome is characterized by hypoparathyroidism, cellular immune deficiency secondary to thymic hypoplasia, congenital heart disease and dysmorphic facial features. In this case report, we describe a 4month old boy who presented w...
متن کاملPrenatal diagnosis and genetic counselling.
Traditionally genetic counselling has been made up of two parts. The first is the establishment of an accurate diagnosis of the disorder, usually in the child of the parents availing themselves of counsel but sometimes in the consultand himself. The second is the calculation of recurrence risks through knowledge or the best possible assumptions about the mode of inheritance of the disease. When...
متن کامل[Kawasaki's disease in remission with cardiac involvement: intrasacular thrombus in a giant aneurism of both coronary arteries. Case report].
Kawasaki disease is of relevance in pediatric practice because it is a systemic vasculitis of unknown origin and the most common cause of acquired heart disease in young patients. Its main complication is the formation of a coronary aneurysm in 25% of patients, unless they receive timely medical treatment. We report the case of a 4 month old male child with Kawasaki's disease, received treatmen...
متن کاملDifficult prenatal diagnosis: fetal coarctation
The prenatal diagnosis of fetal coarctation is still challenging. It is mainly suspected by ventricular disproportion (smaller left ventricle than right ventricle). The sensitivity of ventricular discrepancy is however moderate for the diagnosis of coarctation and there is a high false positive rate. Prenatal diagnosis of coarctation is important because the delivery can be arranged in a centre...
متن کاملPrenatal diagnosis of Ebstein's anomaly.
Ebstein’s anomaly accounts for 0.5% of all congenital heart diseases. The condition is characterized by >8 mm/m2 displacement of the septal and posterobasal tricuspid leaflets toward the apex of the right ventricle (RV). This causes “atrialization” of the RV inflow tract, with decreased size of the RV and right atrial (RA) dilatation. The anterior valve is rarely displaced, but tends to be larg...
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ژورنال
عنوان ژورنال: Ultrasound in Obstetrics & Gynecology
سال: 2019
ISSN: 0960-7692,1469-0705
DOI: 10.1002/uog.21073