Genetic Conditions T

Published Categorized as Genetics
Genetic Conditions T

Thrombocytopenia, a condition characterized by low platelet count, is one of the genetic conditions that affect blood clotting. It can lead to excessive bleeding and bruising and may be inherited or acquired. Dystonia-parkinsonism is another genetic condition that affects movement and can cause involuntary muscle contractions and tremors.

Turner syndrome is a genetic disorder that affects females and is caused by a missing or incomplete X chromosome. It can lead to short stature, infertility, heart defects, and other physical and developmental challenges. Seetyrosine is a rare genetic disorder characterized by elevated levels of the amino acid tyrosine in the blood, which can lead to developmental delays, intellectual disability, and other health problems.

Tangier disease is a rare genetic disorder that affects the body’s ability to transport cholesterol, resulting in a buildup of cholesterol in various tissues and organs. It can cause an enlarged liver and spleen, reduced levels of high-density lipoprotein (HDL) cholesterol, and other health issues. Basal leukodystrophy is a genetic disorder that affects the white matter of the brain and can lead to progressive loss of motor and cognitive abilities.

Seetrimethylaminuria, also known as fish odor syndrome, is a genetic condition characterized by a strong body odor resembling the smell of fish. Osteolysis refers to the progressive loss and destruction of bone tissue, which can be inherited or acquired. TRNT1-related mitochondrial disease is a genetic disorder that affects the function of mitochondria, the energy-producing structures within cells, and can cause muscle weakness, hearing loss, and other symptoms.

Tourette syndrome is a genetic condition characterized by involuntary tics, which are sudden, repetitive movements or vocalizations. Dissection is a genetic condition that affects the connective tissues of the body, leading to the weakening and widening of blood vessels. Lipodystrophy refers to a group of genetic disorders characterized by an abnormal distribution of body fat, which can lead to metabolic problems and other complications.

See also  Kleefstra syndrome

Seetetra-amelia variant is a rare genetic condition characterized by the absence of all four limbs, as well as other abnormalities in the development of the body. Triglyceride storage disease refers to a group of genetic conditions that affect the metabolism and storage of triglycerides, leading to an abnormal accumulation of fat in certain tissues. Purpura fulminans is a severe blood disorder characterized by the formation of blood clots in small blood vessels, leading to tissue damage and organ failure.

Necrolysis refers to the widespread death of skin cells, which can be caused by genetic factors or certain medications. Microcephaly is a genetic condition characterized by an abnormally small head and incomplete brain development. Dystonia is a neurological condition characterized by involuntary muscle contractions and abnormal posture. Insulin resistance is a metabolic disorder that impairs the body’s ability to respond to the hormone insulin, leading to high blood sugar levels. Tetra-amelia is a rare genetic condition characterized by the absence of all four limbs.

Peter Reeves

By Peter Reeves

Australian National Genomic Information Service, including the database of BioManager, has been maintained for a long time by Peter Reeves, a professor at the University of Sydney. Professor Reeves is internationally renowned for his genetic analysis of enteric bacteria. He determined the genetic basis of the enormous variation in O antigens.