Mindblown: a blog about philosophy.
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Is Coronary Artery Disease Genetic?
Explore Coronary Artery Disease and what your DNA can tell you What is coronary artery disease? Coronary artery disease, sometimes called CAD, is a type of heart disease typically caused by the buildup of plaque inside the coronary arteries. The coronary arteries are important because they are the major blood vessels that supply the heart…
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Is Atrial Fibrillation Genetic?
Explore Atrial Fibrillation and what your DNA can tell you What is atrial fibrillation? Atrial fibrillation, sometimes called AFib or AF, is a common type of arrhythmia, or irregular heartbeat. It happens when the two upper chambers of the heart (called the atria) beat irregularly. Normally, the atria pump blood into the two lower chambers…
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Fear of Public Speaking & Genetics
How it works When the brain senses a threat in the environment, a part of the brain called the amygdala responds by activating the “fight or flight” response. This response includes many biological changes, like a faster heart rate and increased blood flow to the brain. Studies have found that when speaking in front of…
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Is MUTYH-Associated Polyposis Genetic?
Explore MUTYH-Associated Polyposis and what your DNA can tell you What is MUTYH-associated polyposis? MUTYH-associated polyposis (MAP) is a hereditary colorectal cancer syndrome. People with MAP tend to develop colon and rectal polyps and have an increased risk of developing colorectal cancer. They may also have a slightly increased risk of developing certain other cancers.…
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Is Chronic Kidney Disease Genetic?
Explore Chronic Kidney Disease and what your DNA can tell you What is chronic kidney disease? Chronic kidney disease is a condition in which the kidneys stop working properly over time. Because the kidneys serve as filters for our blood, chronic kidney disease can cause excess fluid and waste from the blood to build up…
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Pyruvate Kinase Deficiency
What is pyruvate kinase (PK) deficiency? Pyruvate kinase (PK) deficiency is a rare genetic disorder in which red blood cells break down too quickly, leading to chronic anemia. A person must have two variants in the PKLR gene, or two copies of a variant, in order to have this condition. People with just one variant…
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Tyrosinemia Type I & Genetics
What is tyrosinemia type I? Tyrosinemia type I is a rare genetic disorder characterized by high levels of the amino acid tyrosine that can lead to liver and kidney disease. A person must have two variants in the FAH gene in order to have this genetic condition. People with just one variant in the FAH…
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Sjögren-Larsson Syndrome
What is Sjögren-Larsson syndrome? Sjögren-Larsson syndrome is a rare genetic disorder characterized by scaly dry skin, intellectual disability, and persistent muscle stiffness. A person must have two variants in the ALDH3A2 gene in order to have this genetic condition. People with just one variant in the ALDH3A2 gene are called carriers. They’re not expected to…
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MCAD Deficiency
What is MCAD deficiency? MCAD Deficiency is a rare genetic disorder characterized by episodes of very low blood sugar while fasting or under stress. A person must have two variants in the ACADM gene in order to have this genetic condition. People with just one variant in the ACADM gene are called carriers. They’re not…
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Leigh Syndrome, French Canadian Type
What is Leigh syndrome, French Canadian type? Leigh syndrome, French Canadian disorder (LSFC) is a rare genetic disorder. It is characterized by life-threatening periods of lactic acid buildup and brain injury, as well as failure to gain weight. A person must have two variants in the LRPPRC gene in order to have this condition. People…
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