Carine E. deBeaufort

TL;DR: Age/sex-standardised incidence rates for the 0- to 14-year-old age group are reported for 26 European centres that have registered newly diagnosed individuals in geographically defined regions for up to 25 years during the period 1989–2013, suggesting a doubling in incidence rate within approximately 20 years in Europe.

TL;DR: A girl with a prenatal 46,XY karyotype was born with a completely normal female phenotype, including uterus and histologically normal ovaries, which allowed the analysis of the human homolog of M33, Chromobox homolog 2 (CBX2), in this girl to add an additional component to the still incomplete cascade of human sex development.

TL;DR: The Queen Silvia Childrens Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden Department of Pediatrics and the Swedish National Institute of Paediatric Endocrinology and Diabetes, University of Newcastle, New South Wales, Australia Yale School of Medicine, New Haven, Connecticut, USA Department of Psychiatry and Behavioral Sciences, Ann & Robert H. Lurie Children's Hospital of Chicago, Feinberg Schoolof Medicine, Northwestern University, Chicago, Illinois, USA SummitStone Health Partners, Fort Collins, Colorado, USA Riley Hospital for Children, Indiana University School of medicine, Indianapolis, Indiana, USA

TL;DR: In this paper , the authors evaluated access to screening tools for monogenic diabetes in paediatric diabetes centers across the world and its impact on diagnosis and clinical outcomes of children and youth with genetic forms of diabetes.