The KDM6A gene is located in chromosome X and pathogenic variants in this gene are tied to Kabuki syndrome type 2. Even though progress in understanding the functions of KDM6A has been made, its role ...

He had aesthetic flair, buzzed with enthusiasm and adored kabuki — and during his short career, he designed numerous woodcuts featuring its stars and stories. His dominance was such that just ...

The Royal College of Emergency Medicine branded corridor care "dangerous, degrading" and "dehumanising" Every emergency department in Wales is caring for patients in corridors, with the problem ...

Every emergency department in Wales is caring for patients in corridors, with the problem having become "endemic", the Royal College of Emergency Medicine (RCEM) has said. The college, which ...

Bartter syndrome is a group of similar rare conditions that affect the kidneys. It's genetic, meaning it's caused by a problem with a gene. If you have this condition, too much salt and calcium ...

To manage this experience, often called empty nest syndrome, you may need some lifestyle changes or professional help. Share on Pinterest Brat Co/Stocksy United The post-parental stage — which ...

Sudden arrhythmic death syndrome is when someone dies suddenly and unexpectedly from a cardiac arrest, but it's not clear what the cause was. A cardiac arrest is when your heart suddenly stops pumping ...

Potential risks associated with the use of ionizing radiation for imaging and treatment of colorectal cancer in Lynch syndrome patients. Founder vs. non-founder BRCA1/2 pathogenic alleles ...

Study objective There is no consensus on the management of low back pain in the ED and evidence suggests that these patients are likely to receive unwarranted imaging and inappropriate opioid ...

Correspondence to: Dr M Williams University Hospital of North Staffordshire NHS Trust, North Staffordshire Royal Infirmary, Princes Road, Stoke-on-Trent, Staffordshire ST4 7LN, ...

Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene.