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Dementia, Lewy Body (DLB)
Alias:
Lewy Body Dementia
|
Lewy Body Disease
|
Diffuse Lewy Body Disease
|
Dementia with Lewy Bodies
|
Dlb
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Dementia, Lewy Body, Susceptibility to
|
Cortical Lewy Body Disease
|
Autosomal Dominant Diffuse Lewy Body Disease
|
Diffuse Lewy Body Disease with Gaze Palsy
|
Lewy Body Variant of Alzheimer Disease
|
Senile Dementia of the Lewy Body Type
|
Dementia of the Lewy Body Type
|
Lewy Body Type Senile Dementia
|
Dysphasic Dementia Hereditary
|
Lewy Bodies
|
Lewy Body
|
Dlbd
|
Clbd
|
Lbd
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dementia with Lewy bodies (DLB) is a neurodegenerative disorder characterized by dementia, parkinsonism, fluctuating cognitive function, visual hallucinations, falls, syncopal episodes, and sensitivity to neuroleptic medication. Lewy bodies, brainstem or cortical intraneuronal accumulations of aggregated proteins, are the essential pathologic feature. DLB may also exhibit Alzheimer disease-associated pathology and spongiform changes. It is one of the most common types of dementia in older adults, affecting memory, language skills, visual perception, problem-solving, and daily tasks. Lewy bodies, made of alpha-synuclein protein, disrupt brain function, leading to cognitive, movement, and mood issues. The disease progresses over time, with symptoms starting slowly and worsening. Diagnosis can be challenging due to overlapping symptoms with other brain diseases. LBD typically begins at age 50 or older, affecting slightly more men than women. The disease lasts an average of five to seven years from diagnosis to death, with symptoms varying in severity and progression. Treatment may help manage some symptoms, but there is currently no cure. Lewy bodies affect various brain regions, leading to widespread damage and decline in brain functions. Symptoms include REM sleep behavior disorder, dementia, visual hallucinations, and parkinsonism, with individuals requiring increasing assistance as the disease advances.
Related ID:
MALACARDS: DMN031
|
OMIM: 127750
|
MESH: D020961
|
ICD11: 2091156678
Basic Information
Inheritance
Age of Onset
Prevalence
Related Genes
Related Mouse Models
Reference
MALACARDS
AD
Autosomal dominant
Unknown
--
106
1222
92
DMN031
Medical Symptom
Phenotype Information Associated with the Current Disease:
Categorization: Anatomical classification of the disease manifestations.
HPO Frequency/Orphanet Frequency: Indicates the probability of the manifestation occurring in the current disease, allowing sorting by probability.
HPO Source Accession: Links to HPO for detailed manifestation information.
Data Source: HPO, Orphanet
Gene & Mutation
Genes and Mutations Associated with the Current Disease:
Function: Primary biological roles of the genes.
Score: Indicates the strength of the association between the disease and the gene, with higher scores reflecting stronger associations.
Count: Number of mutations associated with the disease-gene pair. The number in parentheses represents the total data points linked to the same ClinVar ID. Clicking the number reveals mutation details.
Data Source: Clinvar
Related Drugs
Drugs Related to the Current Gene, Displaying CAS Number, Status and Phase.
Data Source: Clinical Trials
Related Mouse Models
Mouse Models Related to the Current Gene. Click on the model name to view detailed information.
Data Source: MGI, Cyagen
References Literature
Most Relevant Literature for the Current Gene, Filterable by Year, Article Type, and Sortable by Impact Factor.
Data Source: UniProt, PubMed
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