Searchable abstracts of presentations at key conferences in endocrinology

ea0048cb1 | Additional Cases | SFEEU2017

Primary hyperparathyroidism in a patient with thyroid hormone resistance

Mohamed Isra Ahmed , Carroll Paul

Introduction: Thyroid hormone resistance due to a TRα mutation is rare and only recently described. We report a case of primary hyperparathyroidism in an adult patient with a known TRα mutation.Case presentation: A 60 year old female was referred with hypercalcaemia and hyperparathyroidism that persisted despite correction of vitamin D deficiency. Parathyroid hormone levels continued to be elevated or inappropriately normal with hyper- or normo...

ea0048p12 | Poster Presentations | SFEEU2017

Role of peri-operative psychiatric assessment and intervention in managing the obese patient presenting for bariatric surgery: A complex case of post-bariatric surgery addiction transfer

Mohamed Isra Ahmed , Waller Kathryn , McGowan Barbara

Objective: A case study that demonstrates the importance of thorough psychiatric assessment, intervention and follow-up in morbidly obese patients presenting for Bariatric surgery and risk of addiction transfer.Background: Positive correlation between psychiatric disorders and obesity is documented. Cases of addiction transfer have been reported complicating outcome post Bariatric Surgery.Case description: A 29 year old Caucasian f...

ea0050p285 | Neuroendocrinology and Pituitary | SFEBES2017

Prevalence of paraganglioma at first screen in SDH mutation carriers identified through family screening

Mohamed Isra Ahmed , Velusamy Anand , Izatt Louise , Li Adrian , Joshi Mamta , Breen Louise , McGowan Barbara , Powrie Jake , Obholzer Rupert , Carroll Paul V

Introduction: Mutations in the succinate dehydrogenase gene (SDH) predispose to the development of paraganglioma (PGL) which arise from parasympathetic and extra-adrenal sympathetic-associated chromaffin tissues. Identification of an index case results in family ‘cascade’ screening, often of asymptomatic individuals.Aims: To identify prevalence of PGL tumours and elevated plasma metanephrines at first scre...

ea0050p285 | Neuroendocrinology and Pituitary | SFEBES2017

Prevalence of paraganglioma at first screen in SDH mutation carriers identified through family screening

Mohamed Isra Ahmed , Velusamy Anand , Izatt Louise , Li Adrian , Joshi Mamta , Breen Louise , McGowan Barbara , Powrie Jake , Obholzer Rupert , Carroll Paul V

Introduction: Mutations in the succinate dehydrogenase gene (SDH) predispose to the development of paraganglioma (PGL) which arise from parasympathetic and extra-adrenal sympathetic-associated chromaffin tissues. Identification of an index case results in family ‘cascade’ screening, often of asymptomatic individuals.Aims: To identify prevalence of PGL tumours and elevated plasma metanephrines at first scre...