Searchable abstracts of presentations at key conferences in endocrinology

ea0044ep41 | (1) | SFEBES2016

A rare case of Diabetic ketoacidosis (DKA) in a patient with genetically confirmed maturity onset diabetes of young (MODY)

Mcquade Hannah , Ahmad Sajjad , Stephen Stanaway

Maturity Onset Diabetes of the Young (MODY) accounts for upto 2% of all patients with diabetes. Hepatocyte Nuclear Factor 1 alpha (HNF1-A) MODY is the most common subtype accounting for 30–70% of all MODY cases. Typically, it presents in young adults below the age of 45, frequently < 25 with autosomal dominant family history of diabetes, absence of autoimmune markers and insulin resistance and c-peptide positivity.DKA is a rare complication of M...

ea0041ep713 | Male Reproduction | ECE2016

An audit on evaluation and management of men with hypogonadotrophic hypogonadism in a district general hospital in South-Wales

Hamdan Khaliq , Davies Stephen , Kalhan Atul

Introduction: The current Endocrine Society guidelines (2010) recommend biochemical and radiological evaluation of men with HH to ascertain underlying hypothalamic and/or pituitary aetiology although the cost-effectiveness of this strategy is yet to be established. We did a retrospective audit to ascertain epidemiology, management and diagnostic outcomes for men with HH in our hospital practice against the current Endocrine society guidelines.Methods: A ...

ea0059ep80 | Neuroendocrinology and pituitary | SFEBES2018

A difficult case of Cushing’s disease with unexplained hypertension and rapid metabolic decompensation

Sutton Smith Mark , Cox Jeremy , Robinson Stephen

A 26 year old man of Angolan descent presented to the endocrine clinic with poorly controlled hypertension (systolic blood pressure >200 mmHg). He had been treated with Amlodipine for almost six years, and more recently the addition of Irbesatan and Indapamide had not led to adequate blood pressure control. His hypertension was diagnosed at age 19 and progressive features of Cushing’s disease had remained unnoticed, with truncal striae, easy bruising, myopathy, puffin...

ea0038p480 | Thyroid | SFEBES2015

Thionamide resistant Graves’ disease – it’s not always poor compliance

Ahmad Sajjad , Farooq Ijaz , Stanaway Stephen

A 54 years old female with no significant past medical history was referred by her GP with thyrotoxic symptoms which were not improving on Carbimazole 40 mg daily over the last 3 months in spite of good compliance with the drug. Her initial FT4 was 49.0 pmol/l with TSH suppressed to <0.01 and she was started on Carbimazole 20 mg which a month later was increased to 40 mg/day when there was no improvement in her TFTs. Her TFTs at this point showed FT4 ...

ea0061p005 | (1) | OU2019

Metabolic health and different body composition phenotypes in a Maltese cohort

Agius Rachel , Pace Nikolai , Fava Stephen

It is known that a subset of obese individuals do not exhibit features of the metabolic syndrome (Met-S); these are referred to as being metabolically healthy obese (MHO) individuals. Conversely there are other individuals who although have a normal BMI are insulin resistant and exhibit some of the features of the Met-S and are termed as being metabolically unhealthy normal weight (MUHNW) individuals. This study aims to identify the prevalence of metabolic health among a diffe...

ea0070aep171 | Bone and Calcium | ECE2020

Does real-life time spent within the therapeutic range affect degree of improvement in bone mineral density in men receiving testosterone therapy for hypogonadism?

Osei-Osafo Stephen , Sharma Dushyant , Beeharry Deepa

Background: Hypogonadism in males is associated with a reduction in bone mineral density (BMD). It is known that the reversal of this is achievable through adequate hormone replacement; however, the degree to which this is dependent on the proportion of time patients spend within the recommended therapeutic range (>15 nmol/l) in real-ife has not yet been established.Aim: To evaluate the degree to which the proportion of time that a hypogonadal p...

ea0027p72 | (1) | BSPED2011

Which test to use for screening glucose intolerance in overweight/obese children?

O'Riordan Stephen , Greening James , Shenoy Savitha

Background: With the increasing prevalence of obesity and related morbidity including glucose intolerance in childhood, there remains a dispute about the best screening test to identify this early. The aim of our study was to determine the prevalence of impaired glucose tolerance (IGT)/type 2 diabetes mellitus (T2DM) in a multiethnic cohort of 100 overweight/obese children and adolescents in our clinic and compare the results of the screening tests.Study...

ea0025p277 | Reproduction | SFEBES2011

Increased intensity of P450c17 protein expression in theca cells from polycystic ovaries

Comim Fabio , Hardy Kate , Franks Stephen

Background/aims: Polycystic ovary syndrome (PCOS) is the most common endocrine disorder in women, being characterized by ovarian hyperandrogenism attributed to intrinsic overproduction by theca cells (TCs). Although previous reports pointed a higher stability and transcription of CYP17mRNA (Wickenheisser JK et al. 2006)1, few have examined (and none has quantified) P450c17 protein expression in TCs from PCOS ovaries. Therefore, the aim of this study is to qua...

ea0018p35 | (1) | MES2008

An unusual case of primary infertility

Amin Anjali , Robinson Stephen , Webber Lisa

We present a case of a 29-year-old lady who presented with subfertility. She had had a 2 years history of oligomenorrhoea with highly irregular menses. She had symptoms of depression and described tunnel vision. Clinically, she was euendocrine with no features of hormonal excess or deficiency. She was not hirsute. Visual field testing demonstrated a severe left superior temporal quadrantopia.Laboratory investigations demonstrated an oestriadol level rang...

ea0015p61 | Clinical practice/governance and case reports | SFEBES2008

Like mother like son: a case of maternal and neonatal water intoxication

Simmgen Marcus , Nussey Stephen , Bano Gul

A 37-year old woman developed grand-mal seizures shortly after having given vaginal birth at term. Three hours later, her newborn son also had a tonic-clonic seizure. Following the convulsions, maternal fractures of the humerus and the neck of femur were detected.The pregnancy had been uneventful except for hip pains for 4 weeks prior to delivery. For years, the patient had been ingesting 5 l of bottled water daily. Labour had set in spontaneously and sh...