Miracle Aussie baby beats rare condition in world first

A "miracle" Australian baby has become the first person cured of a rare and deadly brain-melting condition after doctors gambled on an experimental drug tested only on mice, they said Thursday.

The child, known only as "Baby Z", was facing a painful death of and brain damage from molybdenum cofactor deficiency, a which causes a build-up of toxic sulphite and usually kills in months.

But she made an amazing recovery just three days after first being given the untested treatment which was flown in from Germany and rushed through the courts.

"We are looking at her now and she is just an absolute miracle -- she has defied everybody," her mother, who cannot be named for legal reasons, told reporters.

Baby Z started having seizures within 60 hours of her birth in May 2008, prompting her family to appeal to biochemist Rob Gianello to help beat the previously incurable condition which affects just one in a million Australians.

"There was courage and there was death -- we opted for courage," the mother said. "If she wasn't treated she would die a very painful death."

Baby Z's doctor Alex Veldman said Gianello discovered an which had been successfully used on mice by Germany's Gunther Schwarz, but had never been tested on humans.

As Schwarz couriered his entire stock of the compound from Cologne to Melbourne, doctors were in a race against time to get ethics approval from the hospital and a court order clearing its use, with Baby Z worsening by the hour.

"The team ... managed to get this therapy from bench to bedside in about two weeks, a process which normally takes several years," Veldman said.

Within hours of receiving her first dose of the drug, cyclic pyranopterin monophosphate (cPMP), Baby Z's sulphite levels plunged by more than two-thirds and were at normal levels within about three days.

Veldman said Baby Z's alertness improved and her twitching slowed rapidly, with her seizures dropping by 90 percent in three weeks.

"The response was just amazing," he told AFP.

"We can treat this in humans for the first time in (the history of) mankind. It has the potential to save lives all around the world."

Baby Z's development has been slowed by the she suffered before the treatment, and Veldman said she would need a cPMP injection every day for the rest of her life.

But her mother said the baby, now 18 months old, had started speaking and was physically active.

"Every day just gets better and better. We look at her every day and just think, 'Wow'," she said. "(The procedure) was a tiny bit of hope but, when you have nothing, that is a lot of hope."

Veldman said a second child, "Baby P", had since started cPMP treatment in Germany and was "improving rapidly".

The cases were now being analysed ahead of a planned international human trial of the medication at Melbourne's Monash Medical Centre, he said.

(c) 2009 AFP

Explore further

Baby born with 4 eyes and two faces

Citation: Miracle Aussie baby beats rare condition in world first (2009, November 5) retrieved 25 March 2019 from https://medicalxpress.com/news/2009-11-miracle-aussie-baby-rare-condition.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Feedback to editors

User comments

Nov 05, 2009
Lovely news. Kinda. It is still sad that there already was some brain damage, and that the parents and the kid will possibly have to keep paying for constant supply of that medication for the rest of her live. But anything is better than letting her die.

Let's hope for more miracles like this one.

Nov 05, 2009
In a case like this because the baby is the first human treated the drug company will probably provide the drug for free if allowed to do routine tests the rest of it's/her life. I have never heard of a case like this. AWESOME -- chalk one up for science but lets all remember that untested drugs have unheard of side effects -- a chemical building up here a artery disolving there, almost always a liver/kidney issue beacuse it wasn't made to get rid of the drug. But lets all be optimistic

Nov 05, 2009
Hopefully the two weeks wait was just a show for the courts and the doctors administered the drug immediately. I'd be very angry if I grew up and found that I had suffered two weeks of extra brain damage just to appease bureaucrats.

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more