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People with attention-deficit / hyperactivity disorder (ADHD) combined with disruptive behavior disorders (DBDs) share about 80% of genetic variants associated with aggressive and antisocial behaviors.
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Newborns who are diagnosed with phenylalanine hydroxylase deficiency may show no initial symptoms or signs. Over time they may develop symptoms of phenylalanine build-up in
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Genome-wide association studies (GWAS) have typically excluded diverse and minority individuals in the search for gene variants that confer risk of disease. Researchers at Massachusetts
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Hypotonia or weakness of muscles and lack of muscle tone is a symptom of an underlying condition rather than a disease entity in itself. Therapy
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Anxiety disorders are mainly characterized by an unnecessary worry, distress and tension. This may lead to disturbances in concentration, sleep and regular social and work
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PKU or Phenylketonuria is a genetically inherited condition. PKU occurs due to the lack of an enzyme called phenylalanine hydroxylase. This enzyme is a protein.
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Micromanipulation uses microsurgical techniques to study and alter the structure or composition of single living cells or a group of cells under a microscope. It
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Most cases of Moebius syndrome are spontaneous, with no family history and no known genetic cause. In certain rare cases, the disorder has been associated
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Skip to: The Genetics that Underpin Trisomy X Manifestations of Trisomy X Diagnosing Chromosomal Abnormalities in Females Triple X syndrome, also known as 47, XXX,
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