August 14, 2017 <\/p>\n
Sufferers of rare mitochondrial disease have new hope with a new method developed at the University of Sydney. The method provides a diagnosis within weeks instead of months or years through a simple blood sample. <\/p>\n
Mitochondrial diseases are rare and hard to diagnose. They can affect any organ, at any age and are often 'hidden' in other diseases such as diabetes, blindness, liver and kidney failure and even Autism. <\/p>\n
The new method has already led to two new disease gene discoveries where the patients suffered from lactate build-up and hyperglycemia (CYC1), and deafness and organ failure (MRPS7). The research published in the American Journal of Human Genetics and Human Molecular Genetics. <\/p>\n
\"One in 200 people will carry a mitochondrial genetic defect which means nearly 120,000 Australians are at risk of developing serious illness,\" says Minal. \"And yet mitochondrial diseases are extremely difficult to diagnose. They are often referred to as the 'notorious masquerader'\". <\/p>\n
With the faster diagnosis, some people can be treated for what had previously been thought to be untreatable disease. <\/p>\n
For others even if not treatment is available, the diagnosis gives them a cause for the illness and the possibility to enrol in clinical trials. This can result in enormous improvements in quality of life. <\/p>\n
Families can also receive genetic counselling and many may choose to use IVF when building a family, with medical staff able to quantify the risk of the disease being passed on. <\/p>\n
Explore further: New genetic analysis approach could improve diagnosis for mitochondrial disease <\/p>\n
More information: Pauline Gaignard et al. Mutations in CYC1, Encoding Cytochrome c1 Subunit of Respiratory Chain Complex III, Cause Insulin-Responsive Hyperglycemia, The American Journal of Human Genetics (2013). DOI: 10.1016\/j.ajhg.2013.06.015 <\/p>\n
Minal J. Menezes et al. Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia, Human Molecular Genetics (2015). DOI: 10.1093\/hmg\/ddu747<\/p>\n
Newcastle researchers have developed a genetic test providing a rapid diagnosis of mitochondrial disorders to identify the first patients with inherited mutations in a new disease gene. <\/p>\n
French scientists have discovered that supposedly rare mutations in the mitochondria, the 'power plants' of human cells responsible for creating energy, account for more than 7% of patients with a mitochondrial disease manifesting ... <\/p>\n
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Blood test uncovers hidden diseases - Medical Xpress<\/a><\/p>\n","protected":false},"excerpt":{"rendered":" August 14, 2017 Sufferers of rare mitochondrial disease have new hope with a new method developed at the University of Sydney. The method provides a diagnosis within weeks instead of months or years through a simple blood sample Continue reading