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genetics disorders
- When a genetic disorder is diagnosed in a family, family members often want to know the likelihood that they or their children ... the chance of developing or passing on a genetic disorder can be complex. Genetics professionals can help people ...
- ... decisions in the future. In people with a genetic predisposition, the risk of disease can depend on multiple factors in addition to an identified genetic change. These include other genetic factors (sometimes called ... factors. Diseases that are caused by a combination of factors ...
- No; only a small percentage of variants cause genetic disorders—most have no impact on health or development. ... gene. Often, gene variants that could cause a genetic disorder are repaired by certain enzymes before the gene ...
- ... that nearly all conditions and diseases have a genetic component. Some disorders, such as sickle cell disease and cystic fibrosis , ... may be difficult to identify the role of genetics in these disorders, particularly because families often also share environments and ...
- Many genetic disorders result from gene changes that are present in essentially every cell in the body. As a result, ... an individual's health needs. For example, a genetic disorder associated with a heart defect might be treated ...
- ... s chance of developing or passing on a genetic disorder. More than 77,000 genetic tests are currently ... can cause or increase the risk of a genetic disorder. Gene tests can be narrow or large in ...
- Jackson-Weiss syndrome is a genetic disorder characterized by foot abnormalities and the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing ...
- Beare-Stevenson cutis gyrata syndrome is a genetic disorder that typically features skin abnormalities and the premature fusion of certain bones of the skull (craniosynostosis). This early fusion prevents the skull from ...
- ... anticipation. Anticipation is most often seen with certain genetic disorders of the nervous system, such as Huntington's ... become more severe with each successive generation. Most genetic disorders have signs and symptoms that differ among affected ...
- Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the skull ( ...
