SFENCC2019

13:00 - 13:55 
Registration, Tea & Coffee, Posters and Exhibition
13:55 - 14:00 
Welcome and Introduction
14:00 - 15:15 
Clinical Cases 1
14:00

Session starts at 14:00
OC1
Virilisation at puberty – a new subtype in the spectrum of NR5A1 mutations

14:15

Session starts at 14:00
OC2
Explosive onset of primary aldosteronism at puberty, caused by somatic mutation of CTNNB1

14:30

Session starts at 14:00
OC3
A case of Birt-Hogg-Dubé syndrome presenting with a rare oncocytic non-secretory phaeochromocytoma

14:45

Session starts at 14:00
OC4
A novel PHEX mutation, p.(Trp749Ter), is associated with hypophosphataemia and rhabdomyolysis in adulthood

15:00

Session starts at 14:00
OC5
A case of SDHC mutation with two neuroendocrine tumours. Is it just a coincidence?
Ziad Hussein (London)

15:15 - 16:00 
Tea & Coffee, Posters and Exhibition
16:00 - 17:15 
Clinical Cases 2
16:00

Session starts at 16:00
OC6
Effective novel therapy in the use of managing refractory hypoglycaemia in a patient with metastatic insulinoma

16:15

Session starts at 16:00
OC7
An aldosterone crisis
Nicola Tufton (London)

16:30

Session starts at 16:00
OC8
Adenoma to carcinoma progression of a deoxycortisol-secreting adrenal cortical carcinoma in a 71 year old man presenting with hypokalaemia’
Fleur Talbot (Cambridge)

16:45

Session starts at 16:00
OC9
Osteoporosis with a raised serum testosterone – an unexpected finding
Chad Bisambar (Cambridge)

17:00

Session starts at 16:00
OC10
An occult cause of thyrotoxicosis

17:15 - 18:00 
Close, Drinks Reception & Prizes