Boy is world’s first to survive being born with heart outside his body
By LUCY LAING
Last updated at 7:35 PM on 19th February 2012
Comments (69)
Share
When Ryan Marquiss was born with his heart outside of his body, doctors didn’t expect him to survive.
It is an incredibly rare condition and usually babies are stillborn or die within three days.
His heart also hadn’t developed and so he only had half a heart - a combination of defects which is so rare that Ryan is the only one of his kind in the world.
Ryan Marquiss, with his sister Ainsley, has amazed doctors with his survival after being born with his heart outside of his body
Doctors advised his devastated parents to terminate the pregnancy when his mother was just 12 weeks pregnant, but they bravely refused.
And it is a gamble that has paid off, as Ryan is just about to celebrate his third birthday.
Mrs Marquiss, 34, said: ‘We wanted to let nature take its course, so we refused to have the termination.
‘We knew it would be a miracle if he survived the birth but we were unwilling to take matters into our own hands.
‘The doctors told us that no baby with Ryan’s combination of defects had ever survived, so the fact that he is here with us today, is just amazing. He really has astounded everyone.’
Doctors discovered the problem at 12 weeks into his mother’s pregnancy.
The incredibly rare defect, ectopia cordis, affects only eight in every million births and ninety percent of these are stillborn or die within three days.
And adding to that Ryan was also suffering from hypoplastic right heart syndrome, where only the left side of the heart has developed properly.
Mrs Marquiss, who lives with husband Henry, 34, and their other children Natalie, seven, and Ainsley, five, in Pennsylvania, USA, said: ‘All the odds were stacked against him. We knew that it was a miracle that he had been born alive with his heart outside his body, but then to have another life-threatening condition of only having half a heart meant that everything was against him surviving.’
Ryan after the operation, left, and right with his heart outside of his body. The condition is known as ectopia cordis
Doctors at the Children’s National Medical Centre in Washington delivered him at the end of February 2009 by caesarian, helped by a team of 30 medical professionals.
Dr Mary Donofrio, Director of the fetal heart programme at the Children’s National Medical Centre said: ‘If he survived the birth his exposed heart likely would become infected and kill him. Even if infection didn’t happen his heart had one working ventricle and he would require open heart surgery to rewire the blood flow through it.
‘I told the family right from the start that if he survived, it was a miracle.’
Mrs Marquiss said: ‘His heart was protruding out of his chest cavity. The heart was only covered by a thin membrane.
‘But he was alive and we just had to pray that he would carry on fighting.’
Ryan had to have an operation at just two weeks old to have a central shunt placed in his heart to ensure proper blood flow.
Then he underwent more than a dozen operations over the next two years. He had operations to replumb his heart so that the half a heart would do the job of a full size heart. Doctors also put tissue expanders under his skin to produce more skin so they could use it to cover his exposed heart.
Mrs Marquiss said: ‘He has done amazingly well. He has been so brave throughout it, and his sisters have kept him going too. They have been to see him in hospital and made recordings of themselves at home, so Ryan could hear them.
‘He just kept on fighting. He refused to die, and he kept on proving everyone wrong.
‘He will need some sort of chest protection operation in the future but it may be overcome by just wearing some sort of protective padding when he plays sport. He won’t be a competition athlete, but we are hoping he can run around on the playground and climb trees like any other child.’
Ryan’s case has now been reported in a medical journal. Doctors believe that his survival offers hope for other babies with serious heart defects.
In the future he may require a heart transplant, but at the moment, he is progressing well.
Mrs Marquiss said: ‘He really is a medical miracle. When I look at him running around the playground and playing on the climbing wall, I praise God. Every day with Ryan is one we were told we wouldn’t have. So we cherish each moment.’
Follow Ryan’s progress at: http://www.marquissclan.blogspot.com
Comments (69)
Here’s what other readers have said. Why not debate this issue live on our message boards.
The comments below have been moderated in advance.
NewestOldestBest ratedWorst rated
View all
Prenatal testing should be used to help make a plan to help babies who have problems,not as a means to tell the parents to terminate. I am so glad more and more parents are refusing to give up when doctors say to end the pregnancy - just take a look at this happy family as proof that doctors don’t know everything.
- Jennifer, Chandler, AZ, 21/2/2012 05:28
Click to rate Rating 71 Report abuse
OK I’m American but I’m going to type it anyway jolly good well done.
- Robert Wood, Freehold, NJ USA, 20/2/2012 23:13
Click to rate Rating 24 Report abuse
-"I’m glad for this lovely family, but I’m concerned about what will happen in future especially as he may require a heart transplant. Am I right to say his parents were a bit selfish? The ethical question is: is it right to allow this to your child knowing he might not survive, or that if he does, faces a lifetime of care especially if his parents have no problem with fertility. - Pumpin, Birmingham, England, 19/2/2012 12:58” So if you or someone you love dearly develops a disease that will cause you/them a lifetime of problems and will require constant healthcare, are you ok with someone else deciding to terminate your or you loved one’s life for the cost/inconvenience of it all? Just curious as to your level of selfishness when it it comes to your your own life.
- JoeBobHankey, Dallas, Texas, 20/2/2012 16:45
Click to rate Rating 5 Report abuse
May their God bless and keep them. Such a brave little man. Best wishes for a Long, Healthy and Happy future:-)
- Tomlinson, Manchester, 20/2/2012 16:02
Click to rate Rating 34 Report abuse
Lovely story and I love to see kids smile like he is 
- Sally, Derby, 20/2/2012 13:46
Click to rate Rating 28 Report abuse
What a beautiful article - proof to never give up hope, no matter what the odds! His parents are amazing to have had the strength and conviction to go against medical advice. Their happiness is well deserved.
- CG, London, 20/2/2012 13:05
Click to rate Rating 27 Report abuse
We doom our own species with stuff like this. Genetics that can’t survive shouldn’t survive. Is it harsh - yes, but welcome to the world. Don’t get me wrong, I’m happy for the family that he survived and it shows how much surgeons are able to do now, but in the long run, all it will do is make this defect more likely to happen, and more kids will have to survive with only half a heart.
- James, London, 20/2/2012 11:48
Click to rate Rating 91 Report abuse
GOD BLESSED HIM.. WHAT A CUTE LITTLE GUY ))
- Tina, Beirut, Lebanon, 20/2/2012 10:26
Click to rate Rating 29 Report abuse
Awww… the boy is so cute! Great story. Oh, and daddy looks like Mat Damon.
- tate, here, 20/2/2012 06:27
Click to rate Rating 18 Report abuse
I’m also a parent of children who had life-threatening beginnings, so I admire this family’s strength and perserverance for what they went through. And the little guy is simply amazing! Beautiful story…
- jen, toronto, canada, 20/2/2012 05:25
Click to rate Rating 32 Report abuse
The views expressed in the contents above are those of our users and do not necessarily reflect the views of MailOnline.
We are no longer accepting comments on this article.
