ePosters

EA0039P1

Mutations in HS6ST1 cause self-limited delayed puberty (DP) in addition to idiopathic hypogonadotropic hypogonadism (IHH)
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EA0039P2

Islet cell proliferation is inappropriately maintained in the pancreas of children with congenital hyperinsulinism in infancy
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EA0039P3

The relationship between catch up growth and adipokine profile in adolescent children born preterm
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EA0039P4

Use of long acting somatostatin analogue (Lanreotide) in CHI - its pharmacokinetics and long-term follow-up study
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EA0039P5

Junior KICk-OFF (kids in control of food)-developing structured education for primary school age children
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EA0039EP1

Variation in absorption and half-life of hydrocortisone: a need to consider plasma terminal half-life in dosing schedules
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EA0039EP2

Between patient and inter-time point variability in salivary cortisone: cortisol ratios
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EA0039EP3

Cortisol responses to the insulin tolerance test and glucagon stimulation tests in children with idiopathic short stature and idiopathic isolated growth hormone deficiency
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EA0039EP4

Discordance between the cortisol dose for replacement and that required for suppression of androstenedione (A4) and 17 hydroxyprogesterone (17OHP) in congenital adrenal hyperplasia
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EA0039EP5

Current dilution methods cause large variations and inaccuracies when making up 1mcg Synacthen dose
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EA0039EP6

Not always CAH: urine steroid profiling in the investigation and diagnosis of adrenal causes of neonatal hyponatraemia and failure to thrive
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EA0039EP7

Improving patient safety: evaluating the introduction of the Annual Steroid Review and Emergency Alert Systems
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EA0039EP8

Intravenous Etomidate in the management of hypercortisolaemia due to ectopic ACTH producing thymic neuroendocrine tumor
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EA0039EP9

Slow progressing puberty and a secreting adrenocortical tumour in a teenager.
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EA0039EP10

Reducing the risk of adrenal crisis: a service improvement project assessing education on adrenal insufficiency
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EA0039EP11

A case of acute muscular weakness from Ectopic ACTH secreting Neuroendocrine Tumour of the Thymus
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EA0039EP12

A case of a rare adrenocortical tumour mimicking neuroblastoma
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EA0039EP13

Influence of skin colour, ethnicity, and genotype on the response to vitamin D treatment
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EA0039EP14

Increase in lean mass may augment gains in bone mass and size in patients with osteogenesis imperfecta treated with bisphosphonates
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EA0039EP15

The precision of partial image analysis of trabecular bone microarchitecture by high-resolution magnetic resonance imaging in people with childhood-onset bone abnormalities
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EA0039EP16

Metformin regulates the differentiation of murine mesenchymal stem cells via AMPK-independent suppression of p70s6-kinase
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EA0039EP17

The prevalence of fragility fractures in children with cerebral palsy in Manchester: a cross-sectional survey
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EA0039EP18

Trends of use of bisphosphonates in children with secondary osteoporosis
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EA0039EP19

Rickets due to dietary calcium deficiency in Manchester
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EA0039EP20

Early onset cataract in an infant with activating calcium-sensing receptor mutation
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EA0039EP21

Safe prescribing: vitamin D toxicity as a result of inadvertent overdose
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EA0039EP22

Higher glycaemic response after British breakfast cereals in comparison to European breakfasts
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EA0039EP23

Methods used in glycaemic monitoring in children and young people with diabetes in England and Wales
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EA0039EP24

A National survey of annual screening in diabetes clinics in the UK
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EA0039EP25

Using co-production and graphic facilitation to improve patient experience in type 1 diabetes mellitus
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EA0039EP26

Ethnic variation in the correlation between waist-to-height ratio and total daily insulin requirement in children with type 1 diabetes: a cross-sectional study
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EA0039EP27

Junior KICk-OFF - teaching and health care profession working in partnership to develop diabetes education
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EA0039EP28

Is the glycaemic control in type 1 diabetes mellitus affected by Vitamin D status?
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EA0039EP29

Factors influencing type 1 diabetes control in children - a detailed local analysis of an NPDA dataset
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EA0039EP30

Establishing a 'Pump School' in a large children's hospital
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EA0039EP31

Comparison of current trends in obesity in patients with type 1 diabetes in Nottingham with a historical cohort and 2013-2014 national child measurement programme data in the UK
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EA0039EP32

Diabetes distress in transitional age evaluated by 'problem areas in diabetes' in type 1 diabetic patients from Marrakech.
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EA0039EP33

Is the glycaemic control in type i diabetes mellitus affected by Vitamin D status?
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EA0039EP34

Heterozygous glucokinase splicing mutation - identical genotype with variable phenotype in a single family
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EA0039EP35

Retrospective baseline services audit regarding the nature of emergency department attendances by registered diabetic children
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EA0039EP36

Quantity of patient contact with a paediatric diabetes service - is there correlation with HbA1c?
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EA0039EP37

Service evaluation of the 'Ready Steady Go' transition programme in type 1 diabetes in Southampton
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EA0039EP38

Continuous glucose monitoring: effects on metabolic control, fear and frequency of hypoglycaemic episodes
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EA0039EP39

Young people with type 1 diabetes of non-white ethnicity and lower socioeconomic status have poorer glycaemic control in England and Wales - a national population-based study
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EA0039EP40

Pancreatitis, adrenal insufficiency and autoimmune diabetes mellitus in a girl with probable sarcoidosis
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EA0039EP41

Variation in 24-h basal insulin requirements with age in children and young people with type 1 diabetes mellitus
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EA0039EP42

Challenges in diabetic care - the effect of implementing a New Patient Education Programme
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EA0039EP44

Increased insulin requirement may contribute to higher BMI in children and young people with type 1 diabetes mellitus
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EA0039EP45

Decorticate posturing in newly diagnosed case of diabetes ketoacidosis
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EA0039EP46

Evaluation of a novel tool to adjust insulin boluses based on continuous glucose monitoring trend arrows and insulin sensitivity (trend arrow adjustment tool) in children and adolescents with type 1 diabetes using insulin pump therapy
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EA0039EP47

Characteristics of newly diagnosed children with type 1 diabetes - DKA vs Non- DKA presentation
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EA0039EP48

Use of U200 insulin degludec (Tresiba) and metformin in an adolescent with Type-1 diabetes-mellitus
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EA0039EP49

HbA1c: is it a reliable measure of glycaemic control in all patients with type 1 diabetes mellitus?
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EA0039EP50

Monitoring HbA1C in patients on continuous subcutaneous insulin infusion for the treatment of type 1 diabetes
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EA0039EP51

High ferritin and glucose metabolism in diabetes - a case report.
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EA0039EP52

Multi factorial challenges in managing a patient with neonatal diabetes
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EA0039EP53

Too sweet for too long?
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EA0039EP54

A case of a retained needle from insulin pump therapy
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EA0039EP55

Acute kidney injury as a severe complication of diabetic ketoacidosis
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EA0039EP56

Delayed referral of children with new onset type 1 diabetes
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EA0039EP57

Impact of best practice tariff (BPT) for accessing psychological service by diabetic children and young people
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EA0039EP58

Acute hyperglycaemia in cystic fibrosis related diabetes: the role of insulin pumps
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EA0039EP59

Clinical examination of lipohypertrophy: best practice recommendations
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EA0039EP60

To pump or not to pump; paediatric insulin pump efficacy
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EA0039EP61

CYPWMDN diabetes awareness education for schools - regional study day
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EA0039EP62

Frequency of Hypoglycaemia in Children and Young People's Diabetes Clinic
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EA0039EP63

Paediatric type 1 diabetes mellitus in The Gambia, West Africa - presentation and outcome
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EA0039EP64

Audit of DKA admission rates in children and young adults 2010-2015
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EA0039EP65

CASE REPORT-chromosome 9p trisomy with insulin dependent diabetes
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EA0039EP66

Just a little prick; the effect blood glucose monitoring on diabetic control
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EA0039EP67

Severity of presentation with diabetic ketoacidosis at diagnosis of diabetes; India versus the UK
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EA0039EP68

Non-adherence to treatment in teenagers with diabetes: how can we help?
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EA0039EP69

Changes in body composition during late puberty. The effect of sudden sex hormone withdrawal
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EA0039EP70

Chromosomal variations in children and adolescents with gender dysphoria: is routine karyotyping indicated?
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EA0039EP71

Standard GnRH analogue doses do not adequately suppress puberty in adolescent patients
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EA0039EP72

The role of a next generation sequencing panel in the diagnostic pathway in disorders of sex development
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EA0039EP73

Inter and intra-rater reliability of accuracy of testicular volume evaluation: a simulation study
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EA0039EP74

Mode of clinical presentation and delayed diagnosis of turner syndrome
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EA0039EP75

Intravaginal foreign body should be excluded in prepubertal cyclical vaginal bleeding without other evidence of precocious puberty
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EA0039EP76

Causes of precocious puberty in children referred to an Endocrine Unit in Northwest of Turkey
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EA0039EP77

Impact of haematopoietic stem cell transplantation with total body irradiation on apparent bone mineral density in childhood leukaemia survivors
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EA0039EP78

Endocrine sequelae beyond 10 years in survivors of medulloblastoma: comparison of three major treatment regimens
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EA0039EP79

The not so sweet truth of paediatric hypoglycaemia
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EA0039EP80

Volumetric changes in the hippocampus and relationship to memory indices in children with hyperinsulinaemic hypoglycaemia and ketotic hypoglycaemia
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EA0039EP81

Pilot study on the utility and acceptability of video animation as a delivery method for educational materials for families and carers of patients with congenital hyperinsulinism in infancy
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EA0039EP82

Development of a feasible intervention to support communication with young people
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EA0039EP83

Determination of pancreatic hormones in children with different forms of hyperinsulinaemic hypoglycaemia
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EA0039EP84

Congenital hyperinsulinism due to SUR1 (ABCC8) mutation in newborn twins: improvement of clinical outcome after eight years follow-up
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EA0039EP85

Digenic mutation resulting in a rare form of diazoxide responsive congenital hyperinsulinism
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EA0039EP86

The use of glucagon in the treatment of hypoglycaemia due to congenital hyperinsulinism
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EA0039EP87

An incidental finding of an abdominopelvic macrocystic lymphangioma in a girl with Turners syndrome
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EA0039EP88

Usefulness of bedside ketone testing in the evaluation of children with hypoglycaemia
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EA0039EP89

Isolated postprandial hyperinsulinaemic hypoglycaemia in children
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EA0039EP90

Case of raised creatinine in a newborn with congenital hyperinsulinism: diazoxide induced acute kidney injury
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EA0039EP91

Leptin replacement improves central ventilation in a patient with congenital leptin deficiency: first report in childhood
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EA0039EP92

Psychological sequelae in obese paediatric patients and predictors for weight loss
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EA0039EP93

Obesity: a diagnostic dilemma
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EA0039EP94

A modified macronutrient diet for children with Prader-Willi syndrome does work
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EA0039EP95

Effect of dietetic management on weight in children with Bardet-Biedl syndrome
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EA0039EP96

A distinct population of islet cells defines diffuse congenital hyperinsulinism in infancy but not other forms of the disease
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EA0039EP97

Body surface area estimation in girls with Turner syndrome: implications for interpretation of aortic sized index
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EA0039EP98

Cardiovascular assessment in Turner syndrome: current practice in the UK
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EA0039EP99

Positive thyroid peroxidase antibodies at diagnosis of type 1 diabetes mellitus is associated with earlier onset of thyroid disorders
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EA0039EP100

Hypomagnesaemia due to lead poisoning in the context of a heterozygous CLDN-16 mutation
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EA0039EP101

Case series evaluating phenotypical and radiological signs of patients with SHOX mutation
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EA0039EP102

Final adult height and childhood growth trajectories in a cohort of preterm infants
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EA0039EP103

Does better adherence to GH treatment using jet rather than needle delivery translate into improved growth outcomes?
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EA0039EP104

Overcoming the need for a second test: an evaluation of anthropometric, biochemical, and radiological parameters in the diagnosis of GH deficiency
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EA0039EP105

Childhood somatotroph pituitary adenomas due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations
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EA0039EP106

Acid-labile subunit deficiency: a case report
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EA0039EP107

Manifestations of overt diabetes on GH treatment
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EA0039EP108

Achieving a consensus on managing idiopathic thickening of the pituitary stalk through a national multidisciplinary forum, meeting virtually
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EA0039EP109

A rare case of congenital hyperinsulinism associated with hypopituitarism due to pituitary stalk interruption syndrome
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EA0039EP110

Radiolucent hand outline: a simple intervention to improve quality of bone age X-rays
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EA0039EP111

Cost feasibility study: performing GH stimulation test only not full anterior pituitary function tests for simple short stature
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EA0039EP112

Skeletal disproportion in Turner syndrome
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EA0039EP113

Endocrine outcomes in hypothalamic hamartoma: a single-centre study
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EA0039EP114

Growth monitoring in girls attending a tertiary paediatric ENT service with middle ear disease
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EA0039EP115

Growth monitoring and use of growth hormone in children with renal failure
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EA0039EP116

GH deficiency and phenotypic features in four cases of 22q11.2 deletion syndrome
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EA0039EP117

Brain or the kidneys? Nephrogenic Diabetes Insipidus with loss of Pituitary brightness on MRI.
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EA0039EP118

Mosaic form of Turner's can be associated with normal stature and spontaneous puberty: a case report.
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EA0039EP119

Auditing the congenital hypothyroidism (CHT) screening programme in the North East and Cumbria region
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EA0039EP120

Combined hypothyroidism and hypoparathyroidism in an infant following maternal administration of Iodine131 in early pregnancy
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EA0039EP121

Massive pericardial effusion secondary to undiagnosed severe hypothyroidism in a child with neurodisability
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EA0039EP122

Scottish mothers and babies at Yorkhill (MABY) thyroid health study - preliminary report
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EA0039EP123

Apraxia of eyelid and hypothyroidism
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EA0039EP124

Hypothyroidism presenting as child psychosis. A rare finding.
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EA0039EP125

Clinical review of the identification and management of infants born to mothers with thyroid disease - is there a role for routine testing of maternal TRAB in the current practice?
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EA0039EP126

Neonatal thyrotoxicosis - a single centre case series
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EA0039EP127

Combination T3/T4 therapy in paediatric patients with autoimmune hypothyroidism unresponsive to T4 therapy alone
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EA0039EP128

Audit on CH diagnosis and management in UHNM
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Endocrine Abstracts

43rd Meeting of the British Society for Paediatric Endocrinology and Diabetes

EPosters

BiosciAbstracts