Searchable abstracts of presentations at key conferences in endocrinology

ea0034p317 | Reproduction | SFEBES2014

Gestational diabetes and polycystic ovary syndrome

Georgiou Christiana , Mason Helen , Bano Gul

Gestational diabetes mellitus (GDM) poses multiple risks to both the mother and foetus. This includes foetal macrosomia and the development of type 2 diabetes mellitus (T2DM). Women with polycystic ovary syndrome (PCOS) due to their metabolic profile are at greater risk of developing GDM and its long-term sequelae. This study aimed to investigate the prevalence and associations of GDM at St George’s Hospital, with emphasis on women diagnosed with PCOS. The K2 maternal med...

ea0031p312 | Pituitary | SFEBES2013

Metformin treatment of PCOS: St George's Hospital Endocrine Unit Clinical Experience

Walton Hannah , Mason Helen , Bano Gul

Polycystic ovary syndrome (PCOS) is the most common endocrine condition affecting women and is associated with hyperinsulinaemia and hyperandrogenism. Obesity is present in at least 30% of cases and plays a vital role in the development and maintenance of PCOS as well as affecting the severity of the clinical and endocrine features. Significant improvements in symptoms of androgen excess and ovulatory function are seen with even a modest weight loss of 5% in women with PCOS. M...

ea0031p262 | Pituitary | SFEBES2013

Endocrine and radiological abnormalities in empty sella syndrome

Westland Sophie , Mason Helen , Bano Gul , Rich Philip

Background: Primary or idiopathic empty sella syndrome (ESS) is the herniation of the meninges through an incompetent diaphragma sellae into the sella turcica which pushes the pituitary gland aside so giving the appearance of an empty sella. Secondary ESS is caused by damage to pituitary tissue which results in an empty sella turcica. There is significant lack of agreement in the literature regarding the number of patients with empty sella syndrome (ESS) who suffer from pituit...

ea0065p111 | Bone and calcium | SFEBES2019

Hypophosphatasia in an infant: a differential diagnosis that should not be overlooked

Toellner Hannah , Chong Zhuo Min , Srivastava Rajeev , McNeilly Jane , Koppel David , Sangra Meharpal , Shaikh Guftar , McDevitt Helen , Mason Avril , Kinning Esther , Ahmed Syed Faisal

Introduction: Hypophosphatasia is a very rare inherited condition due to ALPL variants and is associated with a variable presentation.Case description: The index case initially presented at 7 months with bulging anterior fontanelle, failure to thrive and mild developmental delay. She was born at 34 weeks gestation and had amniotic bands causing digital anomalies. She was sitting at 8 months, crawling by 15 months and a hearing test was normal. A...