Types of Mitochondrial Diseases
Mitochondrial Disease is an umbrella term for thousands of rare disorders, here is a few of them.
My first Mitochondrial Disease symptoms started when I was 12…
Mitochondrial Disease is an umbrella term for thousands of rare disorders, here is a few of them.
Carnitine Deficiency is when the body can’t produce enough energy from certain fats.
Fatty Acid Oxidation Disorders are caused by faulty genes and they can be fatal for infants.
SCAD Deficiency occurs when certain fats can’t be converted into energy.
The Abel Foundation is a UK based Mitochondrial Disease, founded in 2015.
CPEO is a progressive Mitochondrial Disease that affects the muscles that control the eye.
Since 2005 MitoAction have been supporting the Mitochondrial Disease community.
Beta-Oxidation Defects can happen in most cells in our body and symptoms range from mild to fatal.
Mitochondrial Encephalomyopathies are Mitochondrial Diseases that cause both muscular and neurological problems.
Mitochondrial Myopathies are neuromuscular Mitochondrial Disease’s with symptoms that affect muscles and the nervous system.
The North American Mitochondrial Disease Consortium have created a network for health professionals and patients in North America.
In 2011 it was declared that Luft’s Disease was the rarest identified Mitochondrial Disease.