RECORDED SESSION IMD-S2: Avoiding the Misdiagnosis of Rheumatic Conditions with Other Disorders. What Pediatric Rheumatologists & Pediatricians Should Look for
♦︎ Recorded: Thursday, Nov 22, 2018
♦︎ Language: English
♦︎ Presenter: SYLVIA KAMPHUIS, Pediatric Rheumatologist / Immunologist, Pediatric Infectiology / Immunology/ Rheumatology, Erasmus MC, University Medical Center Rotterdam, NETHERLANDS
♦︎ Learning Objectives: (1) Recognise inborn errors of metabolism that can mimick the clinical phenotype of JIA (2) Learn which key features distinguish genetic disorders from JIA and systemic autoimmune diseases (3) Learn which diagnostics need to be done to rule out genetic (metabolic) disorders
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RECORDED SESSION IMD-S1: Mucopolysaccharidosis type I - Hurler / Scheie and in between
♦︎ Recorded: Wednesday, Nov 21, 2018
♦︎ Language: English
♦︎ Presenter: SUZANNE KIRCHER, Prof.Dr.Dr., MBA, LSD Metabolism, Screening and Genetic Counseling, AUSTRIA
♦︎ Learning Objectives: A short overview about the group of mucopolysaccharide storage diseases with special focus on mucopolysaccharidosis type I (MPS I). (1) What are the typical signs of Hurler patients and what can we see in Scheie patients? (2) How can the diagnosis be confirmed and why is it important for pediatricians as well as medical doctors for adults?
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RECORDED SESSION RHE-S1: Avoiding Misdiagnosis. Clinical Manifestations of Inherited Metabolic Disorders for Pediatric Rheumatologists and General Pediatricians
♦︎ Recorded: Wednesday, Oct 10, 2018
♦︎ Language: English
♦︎ Presenter:ROLANDO CIMAZ, Professor, Head, Meyer Pediatric Hospital, Florence, Department of Health Sciences for Women and Children. ITALY
♦︎ Learning Objectives: (1) Understand how metabolic disease may present to a rheumatologist (2) Review the main musculoskeletal signs of mucopolysaccharidosis (3) Consider the signs and symptoms which should raise a suspicion in the differential diagnosis of JIA
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RECORDED SESSION END-S3: Avoiding Misdiagnosis - Clinical Manifestations of Lysosomal Storage Disorders for Pediatric Endocrinologists and General Pediatricians
♦︎ Recorded: Thursday, Oct 18, 2018
♦︎ Language: English
♦︎ Presenter: NATALIA BELOVA, Pediatric Endocrinologist and Clinical Geneticist, RUSSIA
♦︎ Learning Objectives: (1) Understand how metabolic disease may present to a paediatric endocrinologist (2) Review the main endocrine signs of mucopolysaccharidosis and other metabolic disorders (3) Consider the signs and symptoms which should raise a suspicion in the differential diagnosis to common endocrine condition