REGISTER: Congenital combined pituitary hormone deficiency in Europe webinar

Congenital combined pituitary hormone deficiency (CCPHD) is a rare and heterogeneous disease entity, usually defined as at least two pituitary hormone deficiencies with onset in childhood, without known aquired causes. Variability includes causative gene mutations, clinical onset, hormonal deficiencies, cerebral imaging, neurological impairment and syndromal manifestations.
In this webinar, four European centers ( report on their paediatric and adult cohort data followed by an open discussion led by experts in the field.
Learning objectives
By the end of this webinar, you will be able to:
1. Understand genetic causes to CCPHD and their phenotype correlation
2. Identify patients by clinical presentation in both the neonatal period and later
3. Initiate and continue treatment of CCPHD, including transition
4. Identify and establish support for neurological and syndromal issues