fbpx Prader-Willi Syndrome | HMRI

Dr Vora’s team aims to develop a minimally-invasive diagnostic test to aid with clinical diagnosis and treatment strategy for secondary hypothyroidism in children with the syndrome. The study may help improve personalised treatment of the condition, and may be applicable to children with secondary hypothyroidism due to other medical conditions – for example, after therapy for childhood cancer.  

Researchers 

Dr Komal Vora, A/Professor Patricia Crock, Dr Vicki Maltby

Project type 
Project Grant
Year of funding 
2016