Multiple Fetal Congenital Anomalies | How to Diagnose Cystic Hygroma скачать в хорошем качестве

Multiple Fetal Congenital Anomalies | How to Diagnose Cystic Hygroma

Nuchal translucency is usually done between the 11th and 14th week of pregnancy Increased thickness of the nuchal fold is a soft marker associated with multiple fetal anomalies An increased NT has also been associated with a high risk of miscarriage or fetal death. This risk increases with increasing NT thickness, and miscarriage or fetal death may be preceded by cardiac failure symptoms such as fetal hydrops An increased NT can be associated with a chromosome change such as Down's, cystic hygroma - or lymphangioma - is a birth defect that appears as a sac-like structure with a thin wall that most commonly occurs in the head and neck area of an infant. As the baby grows in the womb, it can develop from pieces of material that carries fluid and white blood cells. The exact cause of a cystic hygroma is unknown. The cyst forms as a result of damage to the lymphatic system during fetal development, Fetal death: 90%. In 10% of cases the fetal karyotype is normal, there are no other obvious defects and the hygromas resolve during pregnancy No medicine can cure cystic hygroma    / @kashifultrasound   #ultrasound #fetalhydrops #cystic hygroma treatment #cystic hygroma fetal death #cystic hygroma of the neck #cystic hygroma ultrasound #fetal nuchal translucency #nuchal scan #nuchal translucency normal range #nuchal translucency screening