MULTIPLE-SCLEROSIS

NEUROLOGY

MSXChange l MS and Women

First episode of Msxchange Dr. Hanaa Keah.
Taking us through the new updated Data in Ms “ menstruation, fertility, pregnancy, Disease-modifying, labor-postpartum, menopause.

Aubagio® - Impact on Brain Health and Real World Efficacy by Dr. Ahmed Shatila

Dr. Shatila; a consultant neurologist at Sheikh Shakhbout Medical City sharing key clinical data of Aubagio® “Teriflunomide”

GAUCHER

RARE-DISEASE

Introduction to Gaucher Disease by Prof. Moeenaldeen D. Alsayed

In this event, which was held on Friday 21st Jan 2022, Prof. Moeen takes us through a journey to introduce Gaucher disease since its discovery in late 19th Century travelling through the overall view of the disease manifestations and the possible disease diagnostic algorithms that might help the physicians in spotting this rare disease with a focus in pediatric patients.

Intro to Multiple Sclerosis by Dr Naji Riachi

Dr. Naji; Professor of Neurology at Sheikh Shakbout Medical city discussing key aspects on Multiple Sclerosis from Epidemiology to prevalence and etiology.

FABRY

Fabry Monitoring Matters Webinar Series

<h3>Renal Monitoring – Dr. Alberto Ortiz (Spain)</h3>
Renal monitoring for patients with Fabry disease as an essential part of the multidisciplinary management of the disease

MUCOPOLYSACCHARIDOSIS-MPS

Dr. Rana Felemban lecture on MPS disease

Consultant Medical genetics talking about early approach of MPS (Who are MPS patients, clinical and diagnostic approach and incidence).

Do not Keep it masked! Prof. Fatih Ezgü

Gaucher disease is a rare genetic disorder passed down from parents to children (inherited). When you have Gaucher disease, you are missing an enzyme that breaks down fatty substances called lipids. Lipids start to build up in certain organs such as your spleen and liver. This can cause many different symptoms. In This lecture, which was held on Friday 21st Jan 2022, Prof. Fatih will take us into some clinical cases of Gaucher disease in children where we will have some real-life experience.

ACID-SPHINGOMYLENASE-DEFICIENCY-NIEMANN-PICK

ASMD: Overview And Clinical Cases - by Prof. Roberto Giugliani

Acid sphingomyelinase deficiency (ASMD), a rare lysosomal storage disease, is an autosomal recessive genetic disorder caused by different SMPD1 mutations. Historically, ASMD has been classified as Niemann-Pick disease (NPD) types A (NPD A) and B (NPD B). In this lecture, Prof. Roberto Giugliani, MD, PhD, will share an overview about ASMD clinical cases to know more about ho to spot this rare diseases.
Dr. Roberto Giugliani, Full Professor at the Department of Genetics of the Federal University of Rio Grande do Sul, is a medical geneticist who founded and is an active member of the Medical Genetics Service of the University Hospital, in Porto Alegre, Brazil. He also founded “House of Rares”, a Brazilian initiative for the care and diagnosis of patients with rare diseases.

A Patient's Journey on Teriflunomide: insights into Long-Term Treatment

Dr. Deeb Khayed is an Adjunct Clinical Assistant Professor at The MBRU School of Medicine, Dubai, UAE and Founding member of the Emirates Neurology Society.

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