Monday 12 May 2014

Photos: Australian Mum Gives Birth To Miracle Conjoined Twins With 2 Brains And One Body

Two girls in one body: Renee Young with her daughters Faith and Hope who were born in a Sydney hospital on Thursday
A very rare condition has resulted in woman giving birth to miracle conjoined twins with two brains in the same skull. The baby appears to have to faces, attached to one neck and body.
Renee Young had been advised to terminate the pregnancy by doctors in Australia ‘because it would be looked upon by the public as a freak’.
But she defied the doctors because Ms Young had never terminated a pregnancy and because they had a family 'that gives us a lot of support'.
Now she and partner Simon Howie, from Sydney, have now welcomed the astonishing little girls – six weeks early.
And they've been given appropriate names – Faith and Hope.
The girls are the result of a rare condition known as disrosopus, where a baby is born with two faces.
The condition is so rare that only 35 cases have ever been recorded and none have survived.
Their father Mr Howie said:
“They are breathing perfectly on their own and feeding,”
“They even had their first bath last night.
“We have no idea how long they will be in hospital. We just want to bring them home, happy and healthy to make our family a little bit bigger and a bit more chaotic.
“Even though there is only one body, we call them our twins
“To us, they are our girls and we love them.”
The couple, who are parents to seven other children, say have braced themselves for a difficult path ahead and refuse to say goodbye to their twins prematurely.
'I would say, if I only get two days with the baby, I only get two days with the baby - at least I have some time with it,' Ms Young said.
Faith and Hope were born with a rare condition called diprosopus, which means they share the same body and organs but have separate brains and two faces
Proud mother: Faith and Hope are now in a stable condition and breathing without support, after initial doubts
'I think they're beautiful and Simon thinks they're beautiful so really that's all that matters,' their mother said.
As the parents of seven other children, Renee and her husband Simon Howie never considered terminating while the girls grew healthy
As the parents of seven other children, Renee and her husband Simon Howie never considered terminating while the girls grew healthy 
The couple refused to terminate their unborn twins despite being warned by doctors of the medical and social problems the girls were likely to suffer
The couple refused to terminate their unborn twins despite being warned by doctors of the medical and social problems the girls were likely to suffer
 The conjoined twins share all their major organs apart from their brains
DIPROSOPUS CONDITION MEDICAL FACTS
The rare condition diprosopus is also known as craniofacial duplication.
Diprosopus refers to a baby born with a single torso, normal limbs and facial features, which are duplicated to a degree.
In mild instances the baby may have a duplicated nose and the eyes may be spaced far apart. But in extreme cases the entire face can be replicated, hence the name diprosopus - Greek for two-faced.
Most babies born with diprosopus are stillborn, and there are fewer than 50 cases documented since 1864.
Where a baby is born with two complete identical faces, the condition is considered a rare variant of conjoined twinning.
But while conjoined twinning is the result of an incomplete separation of two embryos, diprosopus is caused by abnormal activity of the protein Sonic Hedgehog (SHH).
The protein is responsible for signalling craniofacial patterning during embroyonic development, and among other things governs the width of facial features.
Where the protein is found in excess, a baby will have wider facial features, and in extreme cases it can cause the duplication of those features.
Diprosopus can be deteched via ultrasound in pregnancy, or via CT scanning.
One of the first indications of the condition is the detection of abnormally high amount of amniotic fluid present within the amniotoc sac.
There is currently no treatment to cure the condition and because of its rarity few treatment options or corrective surgery techniques exist.
Source: The Embryo Project Encyclopedia

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