Baby girl born with part of her skull MISSING

Desperate parents of a two-month-old baby born with part of her brain and skull missing have today begged for money for life-saving surgery.

Ah Neath’s life is in the balance and her poverty-stricken family are now running out of time and hope that their daughter will survive.

Her mother, Srey, and father, Heang, have frantically tried to scrape funds together and even sold their home to pay for medical care.

However, doctors in Cambodia, where Ah and her family are from, have been unable to treat the condition. Her parents remain hopeful.

Ah Neath’s life is in the balance and her poverty-stricken family are now running out of time and hope that their daughter will survive

Medics in the South-East Asian country, between Thailand and Vietnam, believe the missing part of her skull may have been caused by anencephaly.

The rare condition, sometimes known as ‘open skull’, occurs when the foetus does not form completely while growing in the womb.

Estimates suggest around one in 5,000 babies born each year will have the defect, which also robs them of part of their brain.

Literature states there is no cure for anencephaly and officials at the US Centers for Disease Control warns babies die shortly after birth.

Her mother, Srey, and father, Heang, have frantically tried to scrape funds together and even sold their home to pay for medical care

However, doctors in Cambodia, where Ah and her family are from, have been unable to treat the condition. Her parents remain hopeful

WHAT IS ANENCEPHALY?

Anencephaly, sometimes referred to as ‘open skull’, is a rare birth defect.

It causes parts of a foetus’ brain, scalp and skull to not form completely.

The defect occurs during the third and fourth weeks of pregnancy, according to Cleveland Clinic.

It happens when the neural tube, a channel in the foetus that normally closes to form the spinal cord and brain, doesn’t close as it should.

As a result, children with anencephaly are born without part of their skull and brain. They are often blind and deaf.

Babies with the defect, which strikes one in 5,000 babies each year, tend to die within weeks. There is no cure.

In a desperate attempt to try and save her daughter’s life, Srey has spoken of her fears that her baby girl will die without immediate medical help.

She said: ‘I knew there was something very wrong with my baby when she was born. I have cried for days and asked people to donate money.

‘We are poor and have sold our home and land to try to save my daughter. She is healthy, but her head does not have all of the skull.

‘We are facing hardship and struggling to raise her to survive on the planet. Our only hope is that doctors may be able to help, or a foreign doctor may help.’

Ah was born in February in the remote Tbong Khmum Province – 103 miles (167km) north east of the capital Phnom Penh.

All of her limbs were working fine – but she had a huge crater in the top of her head and a large swelling at the back of it.

She has been in hospital receiving oxygen to support her breathing but has now been discharged and is staying with family.

Ah was born in February in the remote Tbong Khmum Province – 103 miles (167km) north east of the capital Phnom Penh (pictured, a view of eastern Cambodia)

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