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- GM1 Gangliosidosis - Boston Childrens Hospital
GM1 gangliosidosis, also called beta-galactosidase-1 deficiency, progressively destroys nerve cells in the brain and spinal cord Learn more from Boston Children's
- GM1 gangliosidosis | About the Disease | GARD - Genetic and Rare . . .
GM1 gangliosidosis is an inherited lysosomal storage disorder that progressively destroys nerve cells (neurons) in the brain and spinal cord Although the types differ in severity, their features may overlap significantly
- GM1 Gangliosidosis - Cleveland Clinic
GM1 gangliosidosis is a rare disease that causes molecules to build up, irreversibly damaging nerve cells in your brain and spinal cord You inherit a gene change (mutation) from each of your parents that causes this disorder
- GLB1-Related Disorders - GeneReviews® - NCBI Bookshelf
GLB1 -related disorders comprise two phenotypically distinct lysosomal storage disorders: GM1 gangliosidosis and mucopolysaccharidosis type IVB (MPS IVB) The phenotype of GM1 gangliosidosis constitutes a spectrum ranging from severe (infantile) to intermediate (late-infantile and juvenile) to mild (chronic adult)
- Gangliosidosis - Wikipedia
Gangliosidosis Gangliosidosis contains different types of lipid storage disorders [1] caused by the accumulation of lipids known as gangliosides There are two distinct genetic causes of the disease Both are autosomal recessive and affect males and females equally
- GM1 Gangliosidosis—A Mini-Review - PMC
GM1 gangliosidosis is a progressive, neurosomatic, lysosomal storage disorder caused by mutations in the GLB1 gene encoding the enzyme β-galactosidase Absent or reduced β-galactosidase activity leads to the accumulation of β-linked
- Understanding Generalized Gangliosidosis: Symptoms, Causes, and Treatment
Generalized gangliosidosis is a rare genetic disorder that affects the body's ability to break down certain fats and proteins This condition is caused by a deficiency of enzymes that are responsible for breaking down complex molecules called gangliosides
- GM1 gangliosidosis: MedlinePlus Genetics
GM1 gangliosidosis is an inherited disorder that destroys nerve cells (neurons) in the brain and spinal cord This condition can be classified as one of three major types based on the age at which signs and symptoms first appear
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