1.
About Lysosomal Storage Disorders: Disease Classification
Symptoms of some lysosomal storage disorders were first identified as early as the 1880s, and by the early 1900s many LSDs had been described and ...
2.
About Lysosomal Storage Disorders
We have detected that your browser does not have Javascript turned on. ... Outward symptoms of many LSDs often look like symptoms of other more common ...
3.
Sialidosis - Type II (Neonatal / Infantile / Juvenile Onset)
Sialidosis - type II. Select Another Disease ... “Disorders of Glycoprotein Degradation: -Mannosidosis, -Mannosidosis, Fucosidosis, and Sialidosis. ...
4.
Understanding Genetic Diseases: Cells & Enzymes
But just how does the body know how to produce the necessary enzymes in the right amounts? That's encoded in our genetic material in the cell nucleus. ...
5.
LysoSomal Learning
Learn more about lysosomal storage disorders and the science behind the diseases. ... Get detailed clinical information on lysosomal storage disorders, ...
6.
About Lysosomal Storage Disorders: Disease Classification
Symptoms of some lysosomal storage disorders were first identified as early as the 1880s, and by the early 1900s many LSDs had been described and ...
7.
GM1 Gangliosidosis - Type II (Infantile Form)
Enzyme deficiency results in accumulation of GM1 gangliosides in the central nervous system (especially the basal ganglia) and galactosyl oligosaccharides. ...
8.
Tay-Sachs Disease - Type II (Juvenile Form)
Jan 9, 2004 ... Juvenile form begins with ataxia and loss of coordination between 2 and 10 years of age. Speech, cognition, and other motor skills ...
9.
Gaucher Disease - Type III (Chronic Neuronopathic)
Clinical features of type I, plus some of the neurologic complications of type II, although at an older age of onset and slower rate of progression ...
10.
About Lysosomal Storage Disorders
All lysosomal storage disorders share a common pathogenesis: a genetic defect in a specific lysosomal enzyme, receptor target, activator protein, ...
