hrp0097p1-545 | Pituitary, Neuroendocrinology and Puberty | ESPE2023
Baioumi Alaa
, Jayne Farndon Sarah
, Crowne Elizabeth
Background: Paragangliomas are rare tumours that originate from neural crest cells. Diagnosing and managing patients with paragangliomas pose several challenges.Objective: We investigated whether MECP2 defects are associated with an idiopathic CPP phenotype with or without mild neurodevelopmental abnormalities.Clinical presentation: A 14-year-old female presented with cons...