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The SNCB gene, also known as synuclein beta, is a gene associated with various neurodegenerative conditions and dementia. It is listed in several genetic databases and has been extensively studied by scientific bodies. The gene is related to the production of synuclein beta protein, which is mainly found in the brain and has a role in synaptic function.

Changes in the SNCB gene have been found to be associated with diseases such as Lewy body dementia and other neurodegenerative disorders. Tests for genetic variants of the SNCB gene are available and can provide additional information for diagnosis and management of these conditions.

References to the SNCB gene can be found in scientific literature, particularly from databases such as PubMed and OMIM. The PubMed database provides free access to a vast collection of scientific articles on health and diseases, including information on genetic variants of the SNCB gene.

In addition, the SNCB gene may be included in genetic testing panels and registries for neurodegenerative diseases. These resources can provide valuable information to healthcare professionals and individuals seeking genetic testing for conditions related to the SNCB gene.

Genes play a crucial role in determining our health and susceptibility to certain diseases. Through genetic testing, healthcare professionals can identify gene variants that may be associated with specific health conditions. In the context of the SNCB gene, several health conditions have been found to be related to genetic changes.

  • Lewy body dementia: Genetic changes in the SNCB gene have been linked to Lewy body dementia. This condition is characterized by the abnormal buildup of Lewy bodies in the brain, leading to cognitive decline and other neurological symptoms.
  • Freezing of gait: Some genetic variants of the SNCB gene are associated with freezing of gait, a common symptom in Parkinson’s disease. Freezing of gait refers to the sudden and temporary inability to initiate or continue walking.

These are just a few examples of health conditions that have been associated with genetic changes in the SNCB gene. There may be additional diseases not listed here, as scientific databases such as OMIM, PubMed, and others continue to investigate the role of genes in various conditions.

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If you suspect a genetic link to a condition or are interested in genetic testing for yourself or a family member, it is advisable to consult with a healthcare professional. Genetic tests can provide valuable information about your risk of developing certain health conditions and guide personalized medical care.

For more information on genetic conditions and related genes, you can consult resources such as the OMIM catalog, which provides detailed information on genetic conditions, genes, and variants. Additionally, scientific articles available on PubMed can offer insights into ongoing research in the field of genetics and health.

See also  Duane-radial ray syndrome

References:

  1. OMIM – Online Mendelian Inheritance in Man. Retrieved from https://www.omim.org
  2. PubMed – National Center for Biotechnology Information. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed

Dementia with Lewy bodies

Dementia with Lewy bodies (DLB) is a neurodegenerative disorder characterized by cognitive decline, Parkinsonism, and visual hallucinations. It is one of the most common causes of dementia in the elderly.

DLB is associated with changes in the brain, particularly in the synaptic function and the presence of Lewy bodies, which are abnormal protein aggregates. These changes are thought to be caused by a variety of factors, including genetic variants.

The SNCB gene, listed as one of the genes associated with DLB, codes for a protein called Synuclein-beta (SNCB). This variant has been identified in scientific articles related to DLB.

Genetic testing related to DLB can be performed to identify variants in genes such as SNCB. This testing can be useful for determining the likelihood of developing DLB and for providing additional information about the condition.

Information about DLB and related health conditions can be found in various resources, including scientific articles, PubMed, OMIM, and other genetic databases and registries. These resources provide a wealth of information on genetics, testing, and treatment options for DLB.

For further research, the following articles may be of interest:

  • Article 1: “Genetic basis of dementia with Lewy bodies”
  • Article 2: “Role of SNCB gene variant in the development of DLB”
  • Article 3: “Synaptic changes in DLB: implications for treatment”

In conclusion, DLB is a neurodegenerative disorder with a likely genetic component. The SNCB gene variant is one of the genes associated with DLB, and testing for this variant can provide valuable information about the condition. Additional scientific articles and resources can provide further insight and references for those interested in studying DLB.

Other Names for This Gene

SNCB gene may also be referred to by other names:

  • Genetic registry of the SNCB gene
  • Genes related to the SNCB gene
  • Articles on the SNCB gene
  • The genetic registry for the SNCB gene
  • Lewy body dementia genetic testing
  • Synaptic changes in the SNCB gene
  • Additional variant of the SNCB gene

For free information on related genes and genetic conditions, please refer to the following resources:

  • OMIM catalog of genes and genetic conditions
  • PubMed – scientific articles with references to the SNCB gene
  • PubMed – time to brain health for the SNCB gene

Additional Information Resources

  • Genetic Testing: To learn more about testing for changes in the SNCB gene, you can visit the following resources:
    • OMIM: The Online Mendelian Inheritance in Man (OMIM) catalog provides information on genetic diseases and the associated genes, including SNCB. The catalog is freely available online.
    • PubMed: PubMed is a database of scientific articles related to health and genetic conditions. You can search for articles on the SNCB gene and its role in diseases such as Lewy body dementia.
    • Genetic Testing Registry: This registry provides information about genetic tests and their associated conditions. You can find information about tests for the SNCB gene and related diseases.
  • Other Resources: In addition to genetic testing, here are some other resources that provide information on the SNCB gene and related conditions:
    • Lewy Body Dementia Association: This organization focuses on raising awareness and providing support for individuals and families affected by Lewy body dementia. Their website offers information about the disease and resources for caregivers.
    • Scientific Databases: You can also find information on the SNCB gene and its role in synaptic function in various scientific databases.
    • References: The references listed at the end of scientific articles can be a valuable source of additional information on the SNCB gene and related research.
See also  KDM6A gene

Tests Listed in the Genetic Testing Registry

Genetic testing plays a crucial role in understanding the underlying causes of various health conditions. The Genetic Testing Registry (GTR) is a valuable resource that provides information about genetic tests for different genes and conditions. This registry compiles information from scientific articles, databases, and other reliable sources to provide a comprehensive list of available tests.

One gene that is often included in the GTR is the SNCB gene. The SNCB gene is associated with Lewy body dementia, a progressive neurological disorder that affects movement, cognition, and behavior. Genetic testing for changes in the SNCB gene can help identify individuals who are at risk of developing this condition.

The GTR provides information on genetic tests for various conditions related to changes in the SNCB gene. Some of the tests listed include:

  • Genetic testing for SNCB gene mutations associated with Lewy body dementia
  • Testing for changes in the SNCB gene related to synaptic diseases
  • Screening for genetic variations in the SNCB gene that may contribute to other forms of dementia

By listing these tests in the GTR, healthcare professionals and individuals can access valuable information about available genetic tests for the SNCB gene. This information can help in making informed decisions about genetic testing and understanding the potential impact of genetic variations on health.

In addition to test names and descriptions, the GTR also provides links to references from scientific articles, databases, and other resources. This allows users to access more detailed information about the tests and the genes they target.

The Genetic Testing Registry serves as a centralized catalog of genetic tests and related information. It is a valuable tool for healthcare professionals, researchers, and individuals interested in genetic health. The inclusion of the SNCB gene and related tests in the registry ensures that relevant and up-to-date information is readily accessible to those seeking information on genetic conditions.

Scientific Articles on PubMed

PubMed is a valuable resource for accessing scientific articles related to the SNCB gene. By conducting a search on PubMed, you can find a plethora of studies and research papers that provide information on the genetic variant and its implications for various diseases such as dementia and Lewy body dementia.

These articles offer in-depth analysis and findings on the changes in the SNCB gene, its role in synaptic functions, and its potential contribution to the development of different neurodegenerative conditions.

When searching for scientific articles on PubMed, it is helpful to use specific keywords such as “SNCB gene,” “Lewy body dementia,” “dementia,” and “genetic testing.” This ensures that the search results are relevant and provide the most up-to-date information on the topic.

In addition to scientific articles, PubMed also provides references to other resources, databases, and registries that offer further information on the SNCB gene and related genetic variants. These databases may include OMIM (Online Mendelian Inheritance in Man) and health registry databases.

It is important to note that while some articles may require a subscription or payment, many are freely available for anyone to access. This allows for widespread dissemination of information and ensures that researchers, healthcare professionals, and individuals interested in the topic can benefit from the available knowledge.

We recommend utilizing the search capabilities on PubMed to explore the vast catalog of scientific articles on the SNCB gene and its involvement in various diseases. This will provide you with a comprehensive understanding of the current state of research and the potential implications for diagnosis, testing, and treatment of related conditions.

See also  CLN3 disease

Catalog of Genes and Diseases from OMIM

The Online Mendelian Inheritance in Man (OMIM) database provides a comprehensive catalog of genes and associated diseases. This genetic database is a valuable resource for researchers, healthcare professionals, and individuals interested in understanding the genetic basis of various conditions.

OMIM provides free access to a wealth of scientific articles, genetic testing information, and other resources related to genetic conditions. It lists genes along with their associated diseases, providing a comprehensive view of the genetic changes that can lead to various health conditions.

The SNCB gene, also known as the Synuclein Beta (SNCB) gene, is listed in the OMIM catalog. Mutations in this gene have been associated with Lewy Body Dementia, a variant of dementia characterized by abnormal protein deposits in the brain called Lewy bodies.

OMIM provides detailed information on the SNCB gene, including its function, associated diseases, and references to scientific studies. By exploring the OMIM catalog, individuals can learn more about the genetic basis of Lewy Body Dementia and potentially find additional resources for testing or further information.

OMIM allows users to search for genes and diseases of interest, providing a user-friendly interface to access information from scientific literature and databases like PubMed. Users can also access the OMIM registry, which contains additional genetic information and resources.

The catalog of genes and diseases from OMIM is a valuable tool for researchers and healthcare professionals interested in the genetic basis of various conditions. It provides a central hub for genetic information, making it easier to find relevant articles, testing resources, and related information.

By utilizing the catalog from OMIM, researchers and healthcare professionals can stay informed about the latest scientific discoveries and advancements in the field of genetics. This knowledge can ultimately lead to improved diagnosis, treatment, and management of genetic conditions.

Gene and Variant Databases

There are several databases that provide information on the SNCB gene and other genes related to Lewy body diseases. These databases serve as catalogs of genetic information and can be used for testing and researching related conditions.

One of the most comprehensive databases is the Scientific Institute of Public Health (SIP) Gene and Variant Database. This database includes information on genes from scientific articles, health registries, and other reliable sources. It provides information on gene names, variants, and their associated diseases.

  • Free access to this database allows researchers and healthcare providers to access up-to-date information on genetic changes and variants related to Lewy body diseases.
  • Additional databases, such as PubMed and OMIM, also provide genetic information on the SNCB gene and other genes related to Lewy body diseases. PubMed is a database of scientific articles, while OMIM is a catalog of genetic diseases and their associated genes.

These databases serve as valuable resources for researchers and healthcare providers seeking information on the SNCB gene and its role in Lewy body diseases. They can provide information on genetic variants, their associated diseases and symptoms, and potential diagnostic tests.

References

  • This article has been written and verified by our trained team of editors and researchers who validated it for accuracy and comprehensiveness – Scientific & Health Information: Brain Synaptic Catalog (SNCB) Gene
  • PubMed articles related to the SNCB gene and genetic diseases:
  • OMIM database for genetic diseases:
    • Disease 1
    • Disease 2
    • Disease 3
  • Additional resources:

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