Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. The US Food and Drug Administration (FDA) on Monday updated its
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Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. The US Food and Drug Administration (FDA) on Monday updated its
Read morePeople with attention-deficit / hyperactivity disorder (ADHD) combined with disruptive behavior disorders (DBDs) share about 80% of genetic variants associated with aggressive and antisocial behaviors.
Read moreNewborns 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
Read moreGenome-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
Read moreHypotonia or weakness of muscles and lack of muscle tone is a symptom of an underlying condition rather than a disease entity in itself. Therapy
Read moreAnxiety disorders are mainly characterized by an unnecessary worry, distress and tension. This may lead to disturbances in concentration, sleep and regular social and work
Read morePKU or Phenylketonuria is a genetically inherited condition. PKU occurs due to the lack of an enzyme called phenylalanine hydroxylase. This enzyme is a protein.
Read moreMicromanipulation uses microsurgical techniques to study and alter the structure or composition of single living cells or a group of cells under a microscope. It
Read moreMost cases of Moebius syndrome are spontaneous, with no family history and no known genetic cause. In certain rare cases, the disorder has been associated
Read moreSkip 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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