Searchable abstracts of presentations at key conferences in endocrinology

ea0050p372 | Reproduction | SFEBES2017

A rare case of Gestational Hyperandrogenism

Bajwa Hammad , Agha Adnan

A 27 years old primigravida, with no significant past medical history, was referred to Endocrine clinic at 37 weeks gestation with hirsutism. She developed hirsute features during pregnancy and symptoms progressed with advancing gestation. Her physical examination revealed thick coarse dark hair growth in the midline of lower abdomen, between the breasts and forearms. She noted deepening of her voice but denied headaches, visual disturbance or clitromegaly.<...

ea0050p372 | Reproduction | SFEBES2017

A rare case of Gestational Hyperandrogenism

Bajwa Hammad , Agha Adnan

A 27 years old primigravida, with no significant past medical history, was referred to Endocrine clinic at 37 weeks gestation with hirsutism. She developed hirsute features during pregnancy and symptoms progressed with advancing gestation. Her physical examination revealed thick coarse dark hair growth in the midline of lower abdomen, between the breasts and forearms. She noted deepening of her voice but denied headaches, visual disturbance or clitromegaly.<...

ea0050p215 | Diabetes and Cardiovascular | SFEBES2017

A clinical conundrum of euglycaemic ketoacidosis

Bajwa Hammad , Agha Adnan , Salahuddin Sofia

Case History: 37 years old female, presented to Emergency department with worsening SOB over last 24 hours. On systemic enquiry, patient complained of epigastric pain after eating and admitted to un-intentional 22 Kg weight loss in last four months. She clinically appeared dehydrated, with mild epigastric tenderness and no other abnormal signs. She denied any alcohol ingestion or illicit drug use. She had treated Vitamin B12 deficiency and idi...

ea0050p221 | Diabetes and Cardiovascular | SFEBES2017

A rare case of diabetes, hypogonadism and arthritis

Bajwa Hammad , Agha Adnan , Lubina-Solomon Alexandra

We present a challenging case of a 51 years old men, diagnosed with diabetes as he presented to emergency department with osmotic symptoms and hyperglycaemia. He was started on insulin and referred to diabetes clinic.On review, glycaemic control was sub-optimal (HbA1c 94 mmol/mol) and his insulin was changed from biphasic to basal-bolus regimen. His BMI was 21 kg/m2 and no family history of diabetes was report...

ea0050p215 | Diabetes and Cardiovascular | SFEBES2017

A clinical conundrum of euglycaemic ketoacidosis

Bajwa Hammad , Agha Adnan , Salahuddin Sofia

Case History: 37 years old female, presented to Emergency department with worsening SOB over last 24 hours. On systemic enquiry, patient complained of epigastric pain after eating and admitted to un-intentional 22 Kg weight loss in last four months. She clinically appeared dehydrated, with mild epigastric tenderness and no other abnormal signs. She denied any alcohol ingestion or illicit drug use. She had treated Vitamin B12 deficiency and idi...

ea0050p221 | Diabetes and Cardiovascular | SFEBES2017

A rare case of diabetes, hypogonadism and arthritis

Bajwa Hammad , Agha Adnan , Lubina-Solomon Alexandra

We present a challenging case of a 51 years old men, diagnosed with diabetes as he presented to emergency department with osmotic symptoms and hyperglycaemia. He was started on insulin and referred to diabetes clinic.On review, glycaemic control was sub-optimal (HbA1c 94 mmol/mol) and his insulin was changed from biphasic to basal-bolus regimen. His BMI was 21 kg/m2 and no family history of diabetes was report...

ea0044ep42 | (1) | SFEBES2016

Birds of a feather flock together: Maternally inherited diabetes and Deafness AND Mitochondrial encephalopathy lactic acidosis and stroke like episodes

Agha Adnan , Ansari Yousuf , Bajwa Hammad , Webber Jonathan

Introduction: The mutation at m. 3243 adenine to guanine (A>G) in mitochondrial encoded transfer-RNA Leucine 1 (MTTL1) gene is the single most prevalent disease-causing mitochondrial DNA (MtDNA) mutation, with carrier status of 1:400 in our general population. The distinct disease phenotype is dependent on the level of heteroplasmy of wild-type vs mutation-type mtDNA in the specific target tissues, ranging from Maternally inherited diabetes and Deafness (MIDD) to mitochond...

ea0044ep54 | (1) | SFEBES2016

A rare case of type 2 diabetes for 35 years on metformin who developed insulinoma and diazoxide induced renal failure

Alam Muhammad , Agha Adnan , Bajwa Hammad , Mtemrerwa Brian

Background: Insulinoma in a pre existing patient of type diabetes is extremely rare presentation.Methods: We are presenting a a rare case of insulinoma in a pre existing case of type 2 diabetes. A 73 years old patient with type 2 diabetes for 35 years presented to endocrine clinic with hypoglycaemic symptoms ultimatley diagnosed with insulinoma and patient developed renal failure with diazoxide treatment.Result: A 73 years old chin...