Children with neurodevelopmental disorders report congenital abnormalities, such as defects of the heart and/or urinary tract, at least ten times more frequently compared to other children.
May 14, 2024
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Follow-up and treatment of children with cancer is significantly improved when inherited genetic causes are also investigated, according to a new Swedish study. The results of the research involving some 50 researchers and ...
Apr 2, 2024
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About 55 million people worldwide suffer from dementia such as Alzheimer's disease. On Feb. 22, 2024, it was revealed that former talk show host Wendy Williams had been diagnosed with frontotemporal dementia, or FTD, a rare ...
Feb 27, 2024
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Frontotemporal dementia (FTD) is a group of neurologic disorders associated with changes in personality, behavior, language or movement. Some FTD forms are inherited, and some are not. Typically, people develop FTD symptoms ...
Feb 26, 2024
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Many disorders are caused by genetic variants; to make matters worse, the genetic origin of most disorders remains unknown. Now, in a study recently published in the Journal of Clinical Immunology, researchers have shed light ...
Nov 15, 2023
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Scientists have uncovered a genetic explanation for one subset of common brain tumors, according to a study published in Nature Communications.
Oct 27, 2023
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Diseases that run in families usually have genetic causes. Some are genetic mutations that directly cause the disease if inherited. Others are risk genes that affect the body in a way that increases the chance someone will ...
Sep 15, 2023
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Infertility can have genetic causes, but pinpointing the culprit mutations is difficult because fertility and reproduction are controlled by many genes. These genes also carry many harmless but suspicious mutations in different ...
Aug 25, 2023
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The molecular processes responsible for natural aging of cells are poorly understood. Studying conditions in humans where aging is accelerated due to genetic causes presents opportunities to learn about the mechanisms that ...
Jul 13, 2023
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Researchers at the National Institutes of Health and their colleagues have identified genomic variants that cause a rare and severe inflammatory skin disorder, known as disabling pansclerotic morphea, and have found a potential ...
May 31, 2023
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