What is the prevalence of Jejunal Atresia?
How many people does Jejunal Atresia affect? Does it have the same prevalence in men and women? And in the different countries?
Jejunal Atresia is a rare congenital condition characterized by the partial or complete absence of the jejunum, a section of the small intestine. It is estimated to occur in approximately 1 in 1,500 to 1 in 3,000 live births, making it one of the less common gastrointestinal anomalies. Jejunal Atresia is more prevalent in males than females, and it often presents shortly after birth with symptoms like abdominal distension and failure to pass meconium. Prompt surgical intervention is necessary to correct the condition and restore normal intestinal function.
Jejunal Atresia is a rare congenital condition characterized by the partial or complete absence of the jejunum, a part of the small intestine. It occurs during fetal development when the intestines fail to form properly. The exact cause of this condition is unknown, but it is believed to be a result of a combination of genetic and environmental factors.
The prevalence of Jejunal Atresia is relatively low, affecting approximately 1 in 1,500 to 3,000 live births. It is more commonly observed in males than females. Although it is considered a rare condition, it is one of the most common types of intestinal atresia, accounting for about 20% of cases.
Jejunal Atresia often presents shortly after birth with symptoms such as abdominal distension, vomiting, and failure to pass meconium. Prompt diagnosis and surgical intervention are crucial to prevent complications and ensure the baby's well-being. With advancements in medical technology and surgical techniques, the prognosis for infants with Jejunal Atresia has significantly improved over the years.
