Tyla

To make sure you never miss out on your favourite NEW stories, we're happy to send you some reminders

Click 'OK' then 'Allow' to enable notifications

Not now
OK

Doctors make shock diagnosis after mum says newborn looked nothing like her

Ali Condon

Published 
| Last updated 

Doctors make shock diagnosis after mum says newborn looked nothing like her

Featured Image Credit: SWNS

Doctors were able to diagnose a baby with an incredibly rare condition after a mum noticed that her newborn looked nothing like her.

Mum Hannah Doyle, 36, says that her 'mother's instinct' told her something was wrong when she held her baby boy Zander.

He didn't look like her or his dad, and had particularly swollen eyes.

Hannah knew there was something wrong when her newborn looked nothing like her. Credit: SWNS
Hannah knew there was something wrong when her newborn looked nothing like her. Credit: SWNS

After further investigation, Zander was diagnosed with Chromosome Deletion Syndrome, a rare condition that means he has a loss of chromosomes.

Hannah hasn't been able to find anyone who has the same condition yet, so it's not yet known how this condition will affect him in the future.

"When I held him to do skin-to-skin contact, he was just different to my other babies and I instantly knew there was something different," she said.

"When I looked at his eyes, they were very swollen and did look a bit almond like.

"I do believe to this day that it was him telling me, because his eyes look totally different now.

"Now he does look very much like his dad but when he was first born he did look very different."

Zander was diagnosed with Chromosome Deletion Syndrome. Credit: SWNS
Zander was diagnosed with Chromosome Deletion Syndrome. Credit: SWNS

Hannah first became worried about her baby boy when she was just 26 weeks pregnant and was told that Zander had two holes in his heart.

But she was still 'very shocked' when she got his diagnosis.

The mum, who is separated from Zander's father, said: "I was very shocked because I think I had always known that it was a possibility.

"It was a shock and it felt really daunting and really scary because your mind goes into overload and you just start thinking the worst.

"It was harder because there wasn't really much explanation to it.

"The cardiologist was the one that told me the initial diagnosis but he couldn't comment on it or anything."

Loading…

Despite his condition, Zander - now aged 10 weeks - is a 'happy little baby,' though it's now a 'waiting game' to find out how he will be affected in the future.

"That's the hardest thing because with any other medical condition, there's more answers," said Hannah.

"Particularly when I can't find anyone else with the same particular deletion that he's got missing so there's not even anyone else to compare him to.

"It could have no impact on him whatsoever or it could, but the not knowing is hard because you read things and wonder if it will impact him."

Very little is known about Zander's condition. Credit: SWNS
Very little is known about Zander's condition. Credit: SWNS

The single mum of four is trying to spread awareness of Zander's condition, and has started posting videos on TikTok about Chromosome Deletion Syndrome.

"Sometimes I must admit that as a parent, I think it would have been better to have not known this," she shared.

"But I know it's better to know so I can understand him if there is any difficulties so I want to spread awareness so lots of other children are just better understood.

"I think children are so easily labeled and judged for certain behaviours when actually they could be so many more reasons behind that."

Topics: Health, Parenting

Ali Condon
More like this

Chosen for YouChosen for You

Food & Drink

Parmesan cheese isn't made like other cheeses and it's leaving people sick

15 hours ago

Most Read StoriesMost Read

Blake Lively and Justin Baldoni to star in movie adaptation of Coleen Hoover's It Ends With Us

a day ago