Searchable abstracts of presentations at key conferences in endocrinology

ea0074ncc15 | Highlighted Cases | SFENCC2021

A case report on rare metastic Paraganglioma with SDHB mutation

Dhakshinamoorthy Barkavi , Nag Sath , Ahmad Waquar

Paragangliomas are rare neuroendocrine tumours that originate from neural crest cells and can arise from any autonomic ganglion of the body. This is a challenging entity given the limited therapeutic options. Here, we present a rare case of metastatic Paraganglioma in a patient with a germline pathogenic succinate dehydrogenase subunit B (SDHB) mutation. A 54 year old lady was initially diagnosed with functioning bladder paraganglioma with raised metanephrine and norm...

ea0074ncc66 | Highlighted Cases | SFENCC2021

Diagnostic dilemma of cushing disease

Kejem Helmine , Chattington Paula , Mahmud Ahmad

57 year old female physiotherapist, diagnosed with osteoporosis following a fibula fracture from a low impact stretch and a wedge vertebral fracture at age 51 with a metatarsal fracture age 54. With associated history of easy bruising, increase abdominal girth although her weight remained stable at 48.5 kg with BMI 19.9 and proximal myopathy. Blood pressure was constantly normal. Investigations: Early morning random Cortisol 564 and ACTH 6.6 (2–11), cort...

ea0044p230 | Reproduction | SFEBES2016

Serum total cholesterol, thyroid hormone concentrations and haematological variables in cyclic and acyclic Nili-Ravi buffaloes

Ghani Muhammad Usman , Ahmad Ijaz , Ahmad Nazir , Mehfooz Ashar , Ijaz Nabeel

Buffalo is a major dairy animal in many countries of the world, including Pakistan. However, the productive and reproductive performance of this species is affected by many physiological problems such as anestrous. Therefore, this study was conducted to compare serum total cholesterol, thyroid hormone concentrations and haematological variables in cyclic and acyclic Nili-Ravi buffaloes. For this purpose, 60 adult Nili-Ravi buffaloes were divided into two equal groups i.e. cycl...

ea0077p218 | Neuroendocrinology and Pituitary | SFEBES2021

Imaging screening for lung cancer required at diagnosis and at 6 months after established diagnosis of SIADH? A retrospective Audit of real-life clinical practice

Ahmad Waqar , Ahmed Sajeel , Panagiotou Grigorios , Pearce Simon

Background: Syndrome of Inappropriate Anti-diuretic Hormone (SIADH) secretion is the most common cause of hyponatremia in cancer patients. About 14% of hyponatremia in medical inpatients is due to underlying tumor-related conditions. We performed an audit to evaluate prevalence of lung malignancy in patients newly diagnosed with SIADH and to assess proportion of patients having radiological evidence of lung cancer through chest x ray and/or CT chest imaging six months after es...

ea0077p125 | Thyroid | SFEBES2021

Catastrophic complication related to uncontrolled thyrotoxicosis

Sehgal Somanshi , Jain Manushri , Dwivedi Shivangi , Buch Harit , Ahmad Saqib

Presentation: A 32-year-old woman was brought to the Emergency Department following an out-of-hospital cardiac arrest. CPR was started by a neighbour and on arrival, she was found to be in ventricular fibrillation (VF). She received 4 DC-shocks and reverted to atrial fibrillation with fast ventricular rate and staged a full cognitive and haemodynamic recovery. She had a 10-year history of Graves’ thyrotoxicosis for which she was on Carbimazole but remained uncontrolled du...

ea0077lb55 | Late Breaking | SFEBES2021

Optimising diagnostic and management clarity in two opposing sodium centenarians

Chuluunbaatar Yanjinlkham , Dimassi Ahmad , Troke Rachel , Solomon Andrew

Introduction: Hyponatraemia is one of the most common electrolyte abnormalities seen in clinical practice [1] and can be caused by a myriad of aetiologies.Aim: To report two cases of severe hyponatraemia caused by different aetiologies.Case report: A 56-year-old male patient was admitted with 2 episodes of tonic-clonic seizures at his care home. The patient had a background of small cell lung cancer and brain metastases in late 202...

ea0051p024 | Miscellaneous/other | BSPED2017

Using CRISPR/Cas9 gene editing to study molecular mechanisms of congenital hyperinsulinism

Purushothaman Preetha , Aldossary Ahmad , Hart Stephen , Hussain Khalid

Background: Congenital hyperinsulinism (CHI) is a heterogeneous genetically determined condition that is characterised by unregulated secretion of insulin from pancreatic β-cells. The most common and severe cases are caused by mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel subunit. Autosomal recessive mutations in HADH gene are a rare cause of CHI. The advances in CRISPR/Cas9 gene editing technology has enabled the i...

ea0050p194 | Clinical Biochemistry | SFEBES2017

A well recognised but forgotten cause of undetectable Magnesium

Ahmad Sajjad , Akbar Saeed , George Lindsey , Evans Marc

A 74 years old man prsented with gradually worsening confusion with associated jerky movements with background of well controlled type 2 Diabetes, CKD-3, IHD and previous duodenal ulcer. His was on Finasteride, Omeprazole, Mirtazapine, Tamsulocin, Metformin, Atorvastatin, Humulin I insulin. He was taking omeprazole for Duodenal ulcer since 1993.On examination he had jerky movements of the arms suggestive of muscles spasms. Res...

ea0050p365 | Reproduction | SFEBES2017

Effects of feed supplementation with olive oil on serum testosterone, triiodothyronine, thyroxine and some biochemical metabolites in Teddy goat bucks

Farooq Muhammad , Ali Shujait , Jamil Huma , Ahmad Nazir , Ashfaq Khurram

Teddy is a highly proliferative goat breed, as females of this breed are famous for high twinning rates. Feed supplementation of olive oil has been shown to improve semen quality of goat bucks. In this study, the effects of feed supplementation with olive oil on serum testosterone, triiodothyronine (T3), thyroxine (T4) and some biochemical metabolites in Teddy goat bucks were investigated. For this purpose, 9 adult male goats, with clinically normal reproduc...

ea0050p412 | Thyroid | SFEBES2017

A rare case of Moyamoya disease in association with Graves Disease in a Caucasian female

Hasan Faisal , Ahmad Shaza , Chau Fong , Parfitt Vernon

Moyamoya disease is a progressive chronic neurological disease due to multiple narrowing of the carotid arteries. It can be seen in association with atherosclerosis, vasculitis, haematological conditions, connective tissue disease, neurocutaneous syndromes and certain autoimmune diseases. Very few cases have been reported in association with Graves disease and the majority being in the East Asian population. We present a rare case of this association in a young C...