ea0066oc8.5 | Oral Communications 8 | BSPED2019
, Krone Ruth
, Follows Rebecca
, Marks David
, Barrett Timothy
Introduction: PraderWilli Syndrome (PWS) is a rare genetic disorder due to loss of paternally inherited genes on chromosome 15q11-13. It is characterised by neonatal hypotonia, childhood hyperphagia and obesity, hypogonadism, cognitive and behavioural disabilities, and development of scoliosis. PWS multidisciplinary (MDT) clinics were introduced from 2004 at Birmingham Childrens Hospital, a tertiary paediatric centre. This enabled centralised coordination of growth...