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Advanced Course in Rare Lipid Disease - Milan
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Advanced Course on Rare Dyslipidaemia and Atherosclerosis - Importance of Personalized Medicine and Differential Diagnosis

Date: Friday, October 19, 2018

Venue: Bassini Hospital, University of Milan, Via M. Gorki 50, 20092, Cinisello, Balsamo, Milan, Italy.

Aim: The aim of this course is to examine other, rare genetic disorders of lipid metabolism including ß-sitosterolemia; cerebrotendinous xanthomatosis, lysosomal acid lipase deficiency, disorders of high density lipoprotein and familial hypocholesterolemias. While the prevalence of these individual disorders is low, collectively they are important and the busy specialized practitioner will encounter patients with these conditions. Lipidologists need to be familiar with their diagnosis and treatment as they may be associated with high morbidity and mortality. The objective of this course is to review practical aspects of evaluation and management, and to describe real clinical cases of these disorders.

Organized by: SISA Foundation, Italian Society of Atherosclerosis

Endorsed by: European Atherosclerosis Society

Course language: Italian

Audience numbers: 25-35 persons

If you are interested in this course please contact fondazione@sisa.it to learn more and to apply.

Programme

Friday, October 19, 2018  
09.00-09.15  Welcome
09.15-09.30 Rare dyslipidemia introduction  
Alberico L. Catapano, Milan
09.30-10.15 The clinical and experimental laboratory in the study of rare dyslipidemia.
Maurizio Averna, Palermo
10.15-11.00  Genetic and Phenotypic basis of familial chylomicronemia syndrome
Marcello Arca, Rome
11.00-11.15  Coffee break
11.15-11.45 Dysbetalipoproteinemia
Danilo Norata, Milan
11.45-12.30 Homozygous familial hypercholesterolemia. New insights and guidance for clinicians
Maurizio Averna, Palermo
12.30-13.15 Lysosomal acid lipase deficiency.
Laura Calabresi and Monica Gomaraschi
13.15-14.00
Lunch
14.00-14.45 Familial hypocholesterolemias (familial hypobetalipoproteinemia, abetalipoproteinemia, PCSK9 loss of function mutations, familial combined hypolipidemia, and chylomicron retention disease)
Marcello Arca, Rome
14.45-15.30 Rare disorders of HDL metabolism.
Familial hypoalphalipoproteinemia, Tangier disease, and LCAT deficiency. Gaucher disease
Laura Calabresi , Milan
15.30-16.00 The EAS - FHSC Initiative
Alberico L. Catapano, Milan
16.00-16.15 Closing remarks and take-home messages.
Alberico L. Catapano, Milan

Acknowledgement: support for this educational activity has been provided by Alexion.

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