Searchable abstracts of presentations at key conferences in endocrinology

ea0044s5.3 | New frontiers for Vitamin D | SFEBES2016

Prevention and management of nutritional rickets; a 21st century approach

Hogler Wolfgang

Calcium and phosphorus represent the main building material for bone stiffness. The supplier of these bone minerals is the hormone calcitriol, which originates from vitamin D, itself made by sunshine in human skin. Requirement for bone mineral supply is highest during phases of rapid growth, such as in the foetus, infant and pubertal child, making them particularly vulnerable.Deprivation of calcium, whether through low dietary calcium intake and/or low v...

ea0035s19.1 | Osteoporosis - An update | ECE2014

Paediatric osteoporosis

Hogler Wolfgang

Osteoporosis in children is not just BMD and bisphosphonates. Children are unique in their ability to grow and repair bone tissue. Diagnostics, management and the spectrum of osteoporotic conditions encountered in children are different from adults. Children can have primary osteoporosis which are rare diseases like osteogenesis imperfecta (OI), and secondary osteoporosis resulting from chronic conditions or their treatment. Disorders of the bone minerals calcium and phosphate...

ea0033p12 | (1) | BSPED2013

Brown tumours caused by severe vitamin D deficiency: a report of two cases

Ayuk Loveline , Hogler Wolfgang , Shaw Nick

Brown tumours are benign osteolytic lesions of bone caused by high levels of serum parathyroid hormone (PTH). They are now rarely seen as a feature of primary hyperparathyroidism. We report two cases of brown tumour in adolescent girls caused by secondary hyperparathyroidism due to severe vitamin D and dietary calcium deficiency.Case 1: 14.5-year-old South Asian girl referred with a 1 year history of right hip pain. She had presented to the orthopaedic t...

ea0033p68 | (1) | BSPED2013

Multiple pituitary hormone deficiencies in two patients with arthrogryposis multiplex congenita

Narayanan Vidya K , Kirk Jeremy , Hogler Wolfgang

Introduction: Arthrogryposis multiplex congenita is a rare congenital disorder characterised by multiple joint contractures. The association with hypopituitarism has only been reported once before. We report two further children with multiple pituitary hormone deficiencies (MPHD) and arthrogryposis.Case reports: Case 1: this 12-year-old girl was born to consanguineous parents; a previously affected sibling had died. She was dysmorphic with multiple joint...

ea0027p2 | (1) | BSPED2011

Vitamin D supplementation for chronically ill patients: where are we?

Atapattu Navoda , Shaw Nicholas , Hogler Wolfgang

Introduction: ‘At risk’ groups for vitamin D deficiency have long been identified, including the chronically ill. According to guidelines published by the European Society of Endocrinology (ESPE, 2002), the American Academy of Paediatrics (AAP, 2008) and the Endocrine Society (ENDO, 2011), vitamin D levels should be measured in chronically ill or at risk patients. We aimed to test the current knowledge of these guidelines amongst consultants in a large tertiary hospi...

ea0027oc2.6 | Oral Communications 2 (Quick Fire) | BSPED2011

What defines vitamin D deficiency biochemically in children?

Atapattu Navoda , Shaw Nicholas , Davies Paul , Hogler Wolfgang

Background: The level of 25OH vitamin D (25OHD) which separates deficiency from sufficiency is heavily deabted. With decreasing 25OHD levels, typical biochemical derangements set in, such as increasing parathyroid hormone (PTH) and alkaline phosphatase (ALP) levels, and decreasing phosphate and calcium levels. In adults, serum concentrations of PTH reportedly start to rise when serum 25OHD levels drop below 30 μg/l. Such data are scarce in children....

ea0017p27 | (1) | BSPED2008

Long-term outcome of autosomal recessive pseudohypoaldosteronism

Bandhakavi M , Kirk J , Hogler W , Barrett T , Shaw N

Type 1 pseudohypoaldosteronism (PHA1), defined as resistance to aldosterone, is characterised by salt wasting, hyperkalemia and metabolic acidosis and is associated with high renin and aldosterone levels. The autosomal recessive form is characterised by generalised salt wasting and is due to a defect in the epithelial sodium channel. Whilst there are individual case reports on this condition, there are little published data on long-term outcome including neurodevelopment.<...

ea0017p52 | (1) | BSPED2008

Comparison of twice daily insulin and multiple daily insulin regimens in children and adolescents newly diagnosed with type 1 diabetes

Lyder G , Kirk J , Barrett T , Shaw N , Hogler W

Aims: To compare glycaemic control and change in body mass index (BMI) in children and adolescents newly diagnosed with type 1 diabetes (T1D) and started on either twice daily insulin (BD) or multiple daily insulin (MDI).Methods: This study looked retrospectively at all children newly diagnosed with T1D at our hospital from January 2006 to June 2007. There were 44 children and the outcome measures used were change in haemoglobin A1c (HbA1...

ea0051oc4.2 | Oral Communications 4 | BSPED2017

Cumulative radiation exposure from imaging and associated lifetime cancer risk in children with osteogenesis imperfecta

Thorby-Lister Amy , Hogler Wolfgang , Hodgson Kirsten , Crabtree Nicola , Shaw Nick , Saraff Vrinda

Background and objectives: Children with Osteogenesis Imperfecta (OI) require frequent imaging for fractures and surveillance of bone mineral density. Radiation exposure in childhood carries the highest risk of cancer. Here, we estimate the cumulative effective radiation dose (E) and lifetime cancer risk (LAR) from imaging in children with OI. We also explore the hypothesis that the rate of fracture positive imaging for investigation of injuries is related to family history of...