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, European centers will report on their paediatric and adult cohort data followed by an open discussion led by experts in the field.
Agenda

Welcome, Nienke Biermasz, Leiden, NL

Introduction, Henrik Christesen, Odense, DK, 5 min

Genotype-phenotype correlations in CCPHD. Mehul Dattani, London. UK, 10 min

The Finnish paediatric cohort. Taneli Raivio, Helsinki, Finland, 10 min

The French congenital PHD protocol for adults and children. Sarah Castets and Thierry Brue, Marseille, France, 10 min

The Danish National CCPHD cohort with 17 year follow-up. Louise Kjersgaard and Cecilie Jensen, Odense, DK, 10 min

Open discussion. Panelists Evangelia Charmandari, Athens, GR, and Paul vanTrotsenburg, Amsterdam. NL, 15 min.

Closure, Nienke Biermasz, Leiden. NL

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

Webinar summary

WebinarCongenital combined pituitary hormone deficiency in Europe webinar
DateJune 25th, 2025
Time16:00 – 17:00 hr
RegistrationRegistration is closed
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