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Does Gastroschisis have a cure?

Here you can see if Gastroschisis has a cure or not yet. If there is no cure yet, is Gastroschisis chronic? Will a cure soon be discovered?

Gastroschisis cure

Gastroschisis is a birth defect where an infant's intestines protrude through a hole in the abdominal wall. While there is no specific cure for gastroschisis, it can be treated through surgery shortly after birth. The surgical procedure involves placing the intestines back into the abdomen and closing the hole. With prompt medical intervention and ongoing care, many infants with gastroschisis can lead healthy lives.



Gastroschisis is a congenital birth defect that occurs when a baby's abdominal wall does not fully develop during pregnancy. This results in the intestines and sometimes other organs protruding outside the body through a hole near the belly button. It is a rare condition, affecting approximately 1 in every 2,000 to 4,000 live births.



While there is no specific cure for gastroschisis, it can be effectively managed through medical intervention and surgical procedures. The primary goal of treatment is to protect the exposed organs, prevent infection, and promote healthy growth and development of the baby.



Immediately after birth, the baby is placed in a sterile plastic bag or a special silo-like device to protect the exposed organs. This helps to reduce the risk of infection and provides a controlled environment for the organs to gradually return to the abdominal cavity. Surgery is then performed to close the abdominal wall, typically within a few days or weeks after birth.



Post-surgery care is crucial for the baby's recovery. This may involve a period of time in the neonatal intensive care unit (NICU) to monitor the baby's progress, provide nutrition through intravenous fluids or a feeding tube, and address any complications that may arise.



Long-term outcomes for babies with gastroschisis can vary depending on the severity of the condition and any associated complications. With appropriate medical care and support, many children with gastroschisis go on to lead healthy lives. However, some may experience ongoing gastrointestinal issues or require additional surgeries to address complications.



It is important for parents of babies with gastroschisis to work closely with a multidisciplinary medical team, including pediatric surgeons, neonatologists, and other specialists, to ensure the best possible outcome for their child.


Diseasemaps
3 answers
There is no cure but once surgery is complete the survival rate is 90% with few complications later in life.

Posted Aug 10, 2017 by Catharine 600
No not at this time. They are not sure what causes it.

Posted Nov 2, 2017 by Jazmin 2000

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Gastroschisis stories
I'm 25 years old and was born with Gastroschisis, it's been a long road.. I have two beautiful healthy boys that doctors told me I wouldn't be able to have. 
Gastroschisis stories
My daughter Leona was born september 2012. We were 30 weeks and gastroshisis was diagnosed by ultrasound. Till that day, my pregnancy was normal. She was 910g and 37cm. She had 3 surgery. We spend 6 months on NICU. 
Gastroschisis stories
I'l a 30 year old mom of 2 children. My second daughter was born in 2015 with gastroschisis. She was born at 35weeks and 6 says. After the birth she went into surgery, full closure of the tummy. No difficults and now a busy toddler!
Gastroschisis stories
My daughter Cambrie was born with Gastroschisis. We found out at a 20 week ultrasound. She was born at 31 weeks on December 6, 2015. We are lucky she was because her bowels had twisted and had started to cut off blood supply. She spent 3 months in th...
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Found out my son had severe gastroschisis with everything outside of his body (bladder, liver, small and large intestines, etc). He was born at 30 weeks 6 days due to IUGR. He is currently in the NICU now and will have a long fight but we are optimis...

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