Gastroschisis is a rare birth defect where an infant's intestines protrude through a hole in the abdominal wall. It is estimated that the prevalence of Gastroschisis has been increasing over the past few decades. According to studies, the prevalence ranges from 1 in 2,000 to 1 in 4,000 live births worldwide. Although the exact cause is unknown, certain risk factors like young maternal age and tobacco use during pregnancy have been associated with higher prevalence rates. Early diagnosis and appropriate medical intervention are crucial for managing this condition.
Gastroschisis is a rare congenital birth defect characterized by an opening in the abdominal wall, through which the intestines protrude. The exact cause of this condition is unknown, but it is believed to result from a combination of genetic and environmental factors.
The prevalence of Gastroschisis varies across different populations and regions. According to available data, the global prevalence of Gastroschisis has been increasing over the past few decades. In the United States, the prevalence has more than doubled from 3.6 cases per 10,000 live births in the 1980s to around 8.2 cases per 10,000 live births in recent years.
Gastroschisis is more commonly observed in young mothers, particularly those under the age of 20. Additionally, certain risk factors such as smoking, drug use, and inadequate prenatal care have been associated with an increased likelihood of Gastroschisis.
Early diagnosis and prompt medical intervention are crucial for managing Gastroschisis. Treatment typically involves surgical repair of the abdominal wall and careful monitoring of the affected infant's health. With appropriate medical care, the prognosis for infants with Gastroschisis is generally favorable, although long-term complications may arise.