Gm1.lbl.pl - GM1 gangliosidosis - About the Disease - Genetic and Rare …

Provided by Alexa ranking, gm1.lbl.pl has ranked N/A in N/A and 7,966,288 on the world. gm1.lbl.pl reaches roughly 387 users per day and delivers about 11,601 users each month. The domain gm1.lbl.pl uses a Commercial suffix and it's server(s) are located in N/A with the IP number 94.152.134.225 and it is a .lbl.pl domain.

WEBSummary. 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 is caused by genetic changes in the GLB1 gene and is inherited in an autosomal recessive manner.

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GM1 gangliosidosis - About the Disease - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/10891/gm1-gangliosidosis/

WEBSummary. 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 is caused by genetic changes in the GLB1 gene and is inherited in an autosomal recessive manner.

DA: 63 PA: 10 MOZ Rank: 32

GM1 gangliosidosis: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/gm1-gangliosidosis/

WEBDescription. 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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GM1 Gangliosidosis | Boston Children's Hospital
childrenshospital.org

https://www.childrenshospital.org/conditions/gm1-gangliosidosis

WEBGM1 gangliosidosis, also called beta-galactosidase-1 deficiency, is a genetic disorder that progressively destroys nerve cells in the brain and spinal cord. The disorder is one of about 50 diseases classified as lysosomal storage disorders (LSD), where a genetic variation disrupts the normal activity of lysosomes in human cells.

DA: 36 PA: 41 MOZ Rank: 14

GM1 Gangliosidosis—A Mini-Review - PMC - National Center for
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446533/

WEBSep 3, 2021 · 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 galactose-containing glycoconjugates including the glycosphingolipid (GSL) GM1-ganglioside in …

DA: 52 PA: 15 MOZ Rank: 90

GM1 gangliosidoses - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/GM1_gangliosidoses

WEBGM1 is a rare lysosomal storage disorder with a prevalence of 1 to every 100,000 to 200,000 live births worldwide, although rates are higher in some regions. [1] [2] [3] [4] Cause. GM1 Gangliosidoses disorders are caused by mutations in the GLB1 gene, which codes for lysosomal hydrolase, acid beta-galactosidase (β-gal).

DA: 69 PA: 25 MOZ Rank: 17

GM1 Gangliosidosis: Mechanisms and Management - PMC
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044076/

WEBApr 9, 2021 · The lysosomal storage disorder, GM1 gangliosidosis (GM1), is a neurodegenerative condition resulting from deficiency of the enzyme β-galactosidase (β-gal). Mutation of the GLB1 gene, which codes for β-gal, prevents cleavage of the terminal β-1,4-linked galactose residue from GM1 ganglioside.

DA: 100 PA: 2 MOZ Rank: 25

Gangliosidoses - National Institute of Neurological Disorders and Stroke
nih.gov

https://www.ninds.nih.gov/health-information/disorders/gangliosidoses

WEBNov 28, 2023 · The GM1 gangliosidoses are caused by a deficiency of the enzyme beta-galactosidase and has three clinical subtypes: Early infantile GM1 gangliosidosis is the most severe, with onset shortly after birth. Other complications include liver and spleen enlargement, skeletal irregularities, joint stiffness, and distended abdomen.

DA: 27 PA: 81 MOZ Rank: 100

GM1 gangliosidosis type 1 - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/6479/gm1-gangliosidosis-type-1/

WEBGM1 gangliosidosis is caused by genetic changes in the GLB1 gene and is inherited in an autosomal recessive manner. Summary. GM1 gangliosidosis is an inherited lysosomal storage disorder that progressively destroys nerve cells …

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GM1 gangliosidosis type 2 - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/10126/gm1-gangliosidosis-type-2/

WEBGM1 gangliosidosis is an inherited lysosomal storage disorder that progressively destroys nerve cells (neurons) in the brain and spinal cord. The condition may be classified into three major types based on the general age that signs and symptoms first appear: classic infantile (type 1); juvenile (type 2); and adult onset or chronic (type 3).

DA: 48 PA: 55 MOZ Rank: 69

GM1 Gangliosidosis: Mechanisms and Management - PubMed
nih.gov

https://pubmed.ncbi.nlm.nih.gov/33859490/

WEBApr 9, 2021 · The lysosomal storage disorder, GM1 gangliosidosis (GM1), is a neurodegenerative condition resulting from deficiency of the enzyme β-galactosidase (β-gal). Mutation of the GLB1 gene, which codes for β-gal, prevents cleavage of the terminal β-1,4-linked galactose residue from GM1 ganglioside.

DA: 95 PA: 38 MOZ Rank: 4

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Host	Type	Class	TTL	Extra
gm1.lbl.pl	NS	IN	14400	Target: ns1.tld.pl
gm1.lbl.pl	NS	IN	14400	Target: ns2.tld.pl

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IP	94.152.134.225
Domain infomation	No information available about domain name gm1.lbl.pl in the Registry NASK database. WHOIS database responses: https://dns.pl/en/whois WHOIS displays data with a delay not exceeding 15 minutes in relation to the .pl Registry system