Searchable abstracts of presentations at key conferences in endocrinology

ea0029p715 | Diabetes | ICEECE2012

Adding Liraglutide to insulin treated obese type 2 diabetics improves glycaemic control with sustained weight reduction and low hypoglycaemia rate

Jindal R. , Gupta N. , Gupta M. , Siddiqui M. , Wangnoo S.

Aims: To evaluate the effect of Liraglutide on clinical parameters in obese Type 2 diabetic patients with inadequate glycemic control despite treatment with oral hypoglycaemic agents (OHAs) and insulin.Methods: Three hundred and fifty three (M:232, F:121) obese (according to Asian-Indian criteria) type 2 diabetic patients with inadequate glycemic control (HbA1c>7% & <10%) attending outpatients clinic on insulin and OHAs were initiated on lira...

ea0029p204 | Calcium &amp; Vitamin D metabolism | ICEECE2012

Two cases of alendronate induced atypical fracture of femur shaft

Varma T. , Panchani R. , Saini A. , Tripathi S. , Gupta N.

Studies show conflicting results regarding possible excess risk of atypical fractures associated with bisphosphonate (BSP) use. Since BSP reduces bone remodeling, they freeze the skeleton allowing accumulation of microcracks over time leading to atypical fractures. We present two cases of atypical fracture and discuss on monitoring therapy and drug holiday in chronic BSP users.Methods: Over the period of last 8 months we diagnosed two cases of alendronat...

ea0029oc18.2 | Paediatric Endocrinology | ICEECE2012

Clinical profile, gender choice and long term follow up of subjects with 5 alpha-steroid reductase 2 deficiency

Shabir I. , Khurana M. , Eunice M. , Kulshreshtha B. , Khadgawat R. , Gupta N. , Ammini A. , Gupta D.

Introduction: 5 alpha-steroid reductase deficiency (5α SRD) is a rare autosomal recessive disorder. Presented here is the clinical profile and long term outcomes of subjects with 5α SRD examined in our hospital during the last 30 yrs.Methods: Records of patients registered in the endocrine clinic of our hospital and new patients with diagnosis of 5α SRD were compiled. Details of history,physical examination,chromosomal analysis, hormonal s...

ea0029p266 | Calcium &amp; Vitamin D metabolism | ICEECE2012

Primary hypoparathyroidism presenting as adult onset seizure: a report of two cases

Varma T. , Panchani R. , Saini A. , Tripathi S. , Gupta N. , Kumar S\.

Introduction: Primary Hypoparathyroidism presents most commonly in childhood to early adolescence. Disease may be familial or sporadic.Most commonly hypoparathyroidism is secondary to neck operations especially Thyroid surgeries. Primary can be congenital eg- Digeorge syndrome or inherited by AD, AR or X linked mediated.We report 2 cases of late onset seizure due to Digeorge syndrome and Autosomal Dominant Hypoparathyroidism in a elderly lady.Case Report...