lennox gastaut syndrome genetics | Lennox Gastaut Syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
lennox gastaut syndrome genetics	1.77	0.4	6313	28	32
lennox	1.08	0.8	3888	48	6
gastaut	1.22	0.5	661	23	7
syndrome	1.43	0.7	3204	65	8
genetics	0.11	0.7	3548	78	8

Keyword	CPC	PCC	Volume	Score
lennox gastaut syndrome genetics	1	0.5	8976	26
is lennox gastaut syndrome genetic	0.11	0.7	3815	87
lennox gastaut syndrome ncbi	1.27	0.6	3146	19
causes lennox gastaut syndrome	0.08	0.8	3767	43
lennox gastaut syndrome pathophysiology	0.38	0.7	7299	24
lennox gastaut syndrome pubmed	0.11	0.2	5259	45
lennox gastaut syndrome epidemiology	1.89	0.2	315	68
lennox gastaut syndrome in adults	1.81	0.9	5046	26
lennox gastaut syndrome uk	1.09	0.2	4004	47
lennox gastaut syndrome statpearls	0.47	0.9	9358	51
lennox gastaut syndrome definition	0.19	0.3	6792	42
pseudo lennox gastaut syndrome	0.25	0.9	3623	41
lennox gastaut syndrome diagnosis	1.71	0.5	2406	41
define lennox gastaut syndrome	0.2	0.3	1408	50
lennox gastaut syndrome case report	0.83	0.6	5539	22
lennox-gastaut syndrome lgs	0.69	1	6437	9

Search Results related to lennox gastaut syndrome genetics on Search Engine

Lennox Gastaut Syndrome - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK532965/

WEBJul 31, 2023 · Lennox-Gastaut syndrome (LGS) is a rare but severe form of childhood epilepsy. LGS is characterized by a triad of multiple seizure types, characteristic electroencephalogram (EEG) findings, and intellectual impairment.

DA: 92 PA: 67 MOZ Rank: 35

Lennox-Gastaut syndrome: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome/

WEBWhen Lennox-Gastaut syndrome is associated with a genetic change, the variant is usually not inherited but occurs as a random (de novo) event during the formation of reproductive cells (eggs or sperm) in an affected person's parent or during early embryonic development.

DA: 32 PA: 72 MOZ Rank: 45

Lennox-Gastaut Syndrome: In a Nutshell - PMC - National …
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207167/

WEBAug 13, 2018 · Cryptogenic Lennox-Gastaut syndrome was found in the remaining 25% to 35% of patients. Many studies have tried to explain the mystery behind it by coupling the phenotypic description of the epileptic patients and their parents, with genetic studies of …

DA: 97 PA: 37 MOZ Rank: 51

Lennox-Gastaut syndrome - UpToDate
uptodate.com

https://www.uptodate.com/contents/lennox-gastaut-syndrome

WEBJun 5, 2023 · LGS has many causes, including genetic disorders, cortical malformations, tumors, neurocutaneous syndromes (eg, tuberous sclerosis complex), encephalopathies following hypoxic-ischemic insults, meningitis, and head injuries .

DA: 7 PA: 21 MOZ Rank: 64

Characteristics of Genetic Variations Associated With Lennox-Gastaut …
frontiersin.org

https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2020.590924/full

WEBJan 19, 2021 · Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families. Lennox-Gastaut syndrome (LGS) is a severe type of childhood-onset epilepsy characterized by multiple types of seizures, specific discharges on electroencephalography, and intellectual disability.

DA: 3 PA: 96 MOZ Rank: 50

Lennox-Gastaut syndrome - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/9912/lennox-gastaut-syndrome/

WEBLennox-Gastaut syndrome is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing.

DA: 87 PA: 86 MOZ Rank: 61

Lennox-Gastaut Syndrome | Children's Hospital of Philadelphia
chop.edu

https://www.chop.edu/conditions-diseases/lennox-gastaut-syndrome

WEBGenetic causes likely account for a majority of unexplained LGS. Diagnosis of Lennox-Gastaut syndrome. The appearance of multiple types of seizures in early childhood, particularly a combination of tonic, atonic and atypical absence seizures, is a key diagnostic indicator of Lennox-Gastaut syndrome.

DA: 6 PA: 99 MOZ Rank: 87

Characteristics of Genetic Variations Associated With Lennox-Gastaut …
nih.gov

https://pubmed.ncbi.nlm.nih.gov/33584793/

WEBJan 20, 2021 · Keywords: Lennox-Gastaut syndrome; Rare-diseases; epilepsy; genetic variation; whole-exome sequencing. Lennox-Gastaut syndrome (LGS) is a severe type of childhood-onset epilepsy characterized by multiple types of seizures, specific discharges on electroencephalography, and intellectual disability.

DA: 68 PA: 26 MOZ Rank: 52

Lennox-Gastaut Syndrome | National Institute of Neurological …
nih.gov

https://www.ninds.nih.gov/health-information/disorders/lennox-gastaut-syndrome

WEBNov 28, 2023 · Inherited genetic and inherited degenerative or metabolic conditions. No cause can be found in 30 to 35 percent of individuals and Lennox-Gastaut syndrome can be very difficult to treat. A combination of seizure medications and other treatments may be used to improve seizure control and other associated conditions.

DA: 39 PA: 87 MOZ Rank: 7

Lennox-Gastaut syndrome - MedlinePlus
medlineplus.gov

https://medlineplus.gov/download/genetics/condition/lennox-gastaut-syndrome.pdf

WEBCauses. Lennox-Gastaut syndrome can have many different causes. The disorder likely has a genetic component, although the specific genetic factors are not well understood. Most cases of Lennox-Gastaut syndrome develop from an existing neurological abnormality.

DA: 55 PA: 18 MOZ Rank: 75