A one-year-old girl suffering a rare liver disease has stunned doctors with her recovery and is expected to celebrate Christmas at home after spending a quarter of her life in the hospital.
Leia Garcia was born with biliary atresia, a liver disease that has left her near death several times, forcing doctors to scramble to revive her.
The girl from Texas received a liver transplant last month as her only means of survival, though it caused a crucial artery to close, meaning blood was no longer flowing to her liver.
After three failed surgeries to reopen it, to doctors’ surprise the artery began pumping on its own earlier this week and she is expected to be released next Wednesday, two days after Christmas.
Leia’s mother told Daily Mail Online that they’re excited to celebrate the holiday at home even if not on the actual day.
Biliary atresia is a disease of the bile ducts that only occurs in infants.
Bile is a digestive liquid that is made in the liver and travels through the bile ducts to the small intestine, where it helps digest fats.
The disease causes the bile ducts to become inflamed and blocked causing the liquid to remain in the liver and destroy the organ.
Only one out of every 18,000 infants is diagnosed with the disease and it is unknown what causes it.
After Leia was born doctors were able to diagnose her within two weeks when they noticed her liver was enlarged and she wasn’t digesting milk properly.
They checked her billirubin levels, a compound that determines the health of the liver.
While healthy levels for a newborn should read below a one, Leia’s billirubin was at a 20.
At less than a month old she underwent a Kasai procedure, a surgery meant to bypass the bile ducts and prevent liver damage.
However, the surgery was not fully successful and only acted as a band-aid, according to Lei’s mother, Naomi Chacon, 21.
Leia was born on December 10, 2016 and spent her first Christmas in the hospital while recovering from the surgery.
Doctors sent Leia home at one month old and told the family that she would eventually need a liver transplant but needed to weigh at least 20 pounds.
For the next nine months she began developing like any other infant.
‘She was doing everything a normal baby would do, talking and playing but she wasn’t walking or crawling yet,’ Naomi said.
‘They expected her to be on a feeding tube but she went against the odds and bottle fed, which doctors said was rare,’ she added.
But at 10 months old Leia woke up throwing up large amounts of blood.
Her liver was failing rapidly and she was rushed to the hospital where she was put on a breathing tube.
The parents rushed their daughter to the hospital where she was revived by doctors several times and ultimately received a new liver
The transplant caused an artery to close, which pumps blood to the liver, but miraculously the artery has opened on its own and she is expected to go home next week
WHAT IS BILIARY ATRESIA?
Biliary atresia is a rare disease of the liver and bile ducts that occurs in infants.
Only one out of every 18,000 infants is diagnosed with the disease.
With biliary atresia, the liver ducts that produce bile – which flows to the gallbladder – are blocked.
The bile is then trapped inside the liver, quickly causing damage and scarring of the liver cells (cirrhosis), and eventually liver failure.
Signs and symptoms:
- Dark urine
- Acholic (clay-colored) stools
- Weight loss and irritability
Biliary atresia is usually diagnosed through either an ultrasound or a liver biopsy.
There is no medication to treat the disease but there are two forms of treatment.
The first is a Kasai procedure – an operation to reestablish bile flow from the liver into the intestine.
The surgeon removes the damaged ducts outside of the liver and attached a piece of the smaller intestine to the part of the liver that still works so that bile can flow correctly.
The second, a liver transplant, is the definitive treatment for biliary atresia with a high survival rate.