Searchable abstracts of presentations at key conferences in endocrinology

ea0055oc6 | National Clinical Cases | SFEEU2018

Management of T3-toxicosis in pregnancy

Cordiner Ruth , Carty David , Powls Andrew , Mackenzie Fiona , Scott Avril , Gibson Janice , Lindsay Robert

Case history: Pre pregnancy: A 31-year-old female with no family history of thyroid disease presented with clinical hyperthyroidism and large goitre with bruit. Graves’ Disease was confirmed: TSH <0.01 (0.35–5.0 mU/l), free T4 53.4 (9.0–21.0 pmol/l), TSH Receptor Antibodies (TRAB) >40 (0–1.9 U/l), TPO 32.2 (<6 U/ml). She started on carbimazole (CBZ: 20 mg BD) and propranolol. She then switched to propylthiouracil (PTU: 150 mg BD) at 2 months due...

ea0050ep077 | Neuroendocrinology and Pituitary | SFEBES2017

AIP mutation causing familial pituitary tumours

Cordiner Ruth , McManus Frances , Hughes Kate , Panarelli Maurizio , Boyle James , Drummond Russell , Carty David

Familial isolated pituitary adenoma (FIPA) is an increasingly recognised cause of familial pituitary tumours with autosomal dominant inheritance. An increased population risk of AIP mutations has recently been reported in Ireland. We present the cases of three siblings, with likely AIP related disease, attending endocrinology clinics in Glasgow. Patient one has been confirmed to be an AIP mutation carrier.Patient 1 ...

ea0050ep077 | Neuroendocrinology and Pituitary | SFEBES2017

AIP mutation causing familial pituitary tumours

Cordiner Ruth , McManus Frances , Hughes Kate , Panarelli Maurizio , Boyle James , Drummond Russell , Carty David

Familial isolated pituitary adenoma (FIPA) is an increasingly recognised cause of familial pituitary tumours with autosomal dominant inheritance. An increased population risk of AIP mutations has recently been reported in Ireland. We present the cases of three siblings, with likely AIP related disease, attending endocrinology clinics in Glasgow. Patient one has been confirmed to be an AIP mutation carrier.Patient 1 ...