While eating disorders have been widely publicized for decades, far less attention has been given to a related condition called body dysmorphic disorder, or BDD.
Mar 9, 2023
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Pediatric acute myeloid leukemia or pAML is a childhood blood cancer, one that has proved confounding to clinicians and researchers, with a high relapse rate and relatively few identified genetic mutations (compared to the ...
Mar 7, 2023
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The movement disorder ADCY5-related dyskinesia can be treated with the asthma drug theophylline. This has been shown in a recent study by Martin Luther University Halle-Wittenberg (MLU), University Medicine Halle and University ...
Mar 6, 2023
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A Geisinger meta-analysis of recent research on the genetics of cerebral palsy (CP) provides evidence that genetic testing should be offered as the standard of care for people with the disorder, similar to current recommendations ...
Mar 6, 2023
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Multiple sclerosis is characterized by an immune system gone haywire. A patient's immune system starts treating the protective coating of the nerves—called myelin—as dangerous. The subsequent nerve damage can cause a ...
Mar 1, 2023
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Northwestern Medicine scientists have identified the cause of a genetic subtype of autism and schizophrenia that results in social deficits and seizures in mice and humans.
Feb 28, 2023
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Genetic risk factors for major depression (MD), bipolar disorder (BD), other nonaffective psychosis (ONAP), and schizophrenia are systematically associated with their diagnostic trajectories, according to a study published ...
Feb 22, 2023
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A team of medical scientists at the Max Planck Institute for Psycholinguistics has found structural differences in white matter in the human brain that can be linked to genetic variants that may be responsible for some behavioral ...
T-cells that are part of our immune system are central in the protection against infections and cancer. With the help of TCRs, the cells recognize foreign invaders and tumor cells.
Feb 15, 2023
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Universitätsmedizin Berlin, the Max Planck Institute for Molecular Genetics (MPIMG), and the University Hospital Schleswig-Holstein (UKSH) have investigated in detail how BPTA syndrome, an extremely rare hereditary condition, ...
Feb 8, 2023
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