Staff from the Western Australian Institute for Medical Research (WAIMR), the Telethon Institute for Child Health Research (TICHR) and the Neurogenetics and Forensic laboratories within PathWest, combined to establish that the little girl had died from the devastating neurological disorder, Rett Syndrome.
The group was able to make the diagnosis after carrying out a gene test on DNA extracted from the baby tooth.
A paper outlining the effort has just been published in the international medical journal, The Lancet.
Professor David Ravine, from WAIMR's Laboratory for Molecular Genetics and Dr Helen Leonard, coordinator of the Australian Rett Syndrome Study at the TICHR in Perth, said confirming the diagnosis had finally laid to rest many of the family's fears.
"Despite intensive investigation, the little girl's condition went undiagnosed by doctors all through her life, so the fact that the cause of her illness and death was finally pinpointed, gave the family the information they needed to understand what had happened," said Professor Ravine.
The mother contacted Dr Helen Leonard after coming across the Australian Rett Syndrome Study website and remembering that an occupational therapist had once suggested that her daughter might have this disorder.
Dr Leonard said that the confirmation of a definite diagnosis had erased years of worry for the family.
"Not knowing what was causing their daughter's illness, her parents began to wonder if they were somehow responsible," she said.
"They were worried their daughter's condition may be linked to a vaccination she'd had just before her health deteriorated.
"On top of that, her father felt guilty about the circumstance of a fall she'd had at 17 months. "So to know, after such a long time, what had caused their daughter's illness was a tremendous relief to them." Professor Ravine said that the mother's search for an explanation, even after her daughter's death, was prompted by concerns that any future grandchildren might be affected.
"Now, more than 10 years after her daughter's death, the test finding has discounted fears that the couple's son could also pass the condition on to any children he might have," said Professor Ravine.
He said that although extracting DNA from unconventional sources such as teeth was common in forensic medicine, it was not often used in a case such as this.
"Using this sort of technique in genetic counselling situations is very rare, but given that it's technically simple to do, and has had such enormous benefits for the family, I suspect it could become more common," he said.
The Australian Rett Syndrome Study is a nation-wide study of Rett syndrome that is directed from the Telethon Institute for Child Health Research. It involves a collaboration of centres across Australia with the common goal of being able to provide accurate information about the progression of the disorder and about how it can best be managed. The study is also researching the relationship between the clinical and genetic characteristics of Rett syndrome and is an international leader in this area.
BACKGROUND INFORMATION
MEDIA CONTACTS:
Natalie Papadopoulos
WAIMR
M: +61 407 984 435
Elizabeth Chester
Telethon Institute for Child Health Research
M: +61 409 988 530