From November 1st
to December 1st
is accepting late-breaking abstracts for WORLDSymposium
2018 being held February 5-9, 2018 in San Diego.
is THE research conference for people interested in lysosomal disease research. Last year, more than 1600 participants from over 50 countries attending the meeting and this year will likely be even bigger.
Abstracts focused on basic, translational, or clinical research are all accepted. The only speculation is that it involves a lysosomal disease.
Lysosomal Diseases or lysosomal storage diseases are a group of rare inherited disorders that result from defects in lysosomal function. Lysosomes are cellular vesicles that degrade large molecules. Generally, people with lysosomal disease are missing a key enzyme involved in that degradation process and the end result is usually a buildup of molecules in the cells that leads to multi-organ damage. Each lysosomal disease is associated with a specific enzyme and the corresponding molecule that accumulates in the body will determine the symptoms.
Some of the lysosomal diseases include:
- Alpha-mannosidosis types I & II
- Batten disease
- Cholesteryl ester storage disease
- Fabry disease
- Galactosialidosis types I & II
- Gaucher disease
- Krabbe disease
- Neuronal ceroid lipofuscinosis (infantile, late infantile, juvenile)
- Mucolipidosis types II, III, & IV
- Mucopolysaccharidosis type I (Hurler, Hurler–Scheie, and Scheie)
- Mucopolysaccharidosis type II (Hunter syndrome)
- Mucopolysaccharidosis type III (Sanfilippo syndrome)
- Mucopolysaccharidosis type IV ( Morquio syndrome)
- Mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome)
- Niemann-Pick disease
- Pompe disease
- Sandhoff disease
- Schindler disease
- Sialidosis types I & II
- Tay-Sachs disease
- Wolman disease
Abstracts must be less than 300 words and cannot contain images or figures.
To submit a late-breaking abstract, click here.
Look for Rare Disease Report’s coverage of the upcoming conference at www.raredr.com/conferences
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