Stephany Donze

Stephany Donze is a Researcher in the Clinical Genetics department at Erasmus MC, focusing on genetic syndromes and endocrine disorders. Her work primarily revolves around Prader-Willi Syndrome (PWS), investigating growth hormone treatments, metabolic biomarkers, and associated comorbidities such as scoliosis and bone density issues. She collaborates extensively on clinical trials evaluating long-term treatment outcomes and diagnostic methodologies.

Research interests include genetic diagnostics in prenatal settings, HPA axis dysfunction in pediatric populations, and the impact of growth hormone therapies on skeletal health. Her studies emphasize longitudinal analyses of treatment efficacy and biomarker development for PWS management.