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Task-specific focal dystonia

Task-specific focal dystonia is a rare neurological condition that affects the control of specific movements. It is also known as occupational dystonia or writer’s cramp, as it often occurs in individuals who perform repetitive hand movements, such as writing or playing a musical instrument.

The history of task-specific focal dystonia can be traced back to the late 19th century, when it was first described by neurologists. Since then, research and advocacy organizations such as the Dystonia Medical Research Foundation, the Dystonia Coalition, and the National Institute of Neurological Disorders and Stroke have provided support and information to affected individuals and their families.

Task-specific focal dystonia can be caused by a combination of genetic and environmental factors. Several genes have been identified that may play a role in its development, and research is ongoing to further understand the causes and potential treatments for this condition. The frequency of task-specific focal dystonia in the general population is estimated to be around 1 percent.

ClinicalTrials.gov provides additional information about ongoing clinical trials and research studies related to task-specific focal dystonia. Many articles and case studies have been published on this topic, and references to these can be found in scientific journals and databases such as PubMed and OMIM.

Individuals affected by task-specific focal dystonia often experience muscle cramps and involuntary movements in the affected area, such as the hand, wrist, or arm. These symptoms can be debilitating and may significantly impact daily activities and quality of life.

While there is no cure for task-specific focal dystonia, treatments such as physical therapy, medications, and botulinum toxin injections can help manage the symptoms and improve function. It is important for individuals with task-specific focal dystonia to work closely with healthcare professionals to develop a personalized treatment plan.

Patients, too, are unhappy with the care they receive during those brief interactions with their doctors. Healthcare communications company West Corporation reported that 25% of patients don’t feel that their provider cares about them as an individual and nearly 20% aren’t convinced their doctor is focused on improving their health – even though 93% of doctors strongly agree that patient satisfaction is important.

Frequency

The frequency of task-specific focal dystonia varies depending on the specific task and population studied. For example, writer’s cramp is estimated to affect 1 to 3 percent of the general population, but the prevalence may be higher among professional writers and musicians.

In golfers, a specific form of task-specific dystonia, the frequency is lower, with an estimated prevalence of 0.5 to 1 percent among this population.

While task-specific focal dystonia is relatively rare compared to other movement disorders such as Parkinson’s disease or essential tremor, it is an important clinical entity that significantly affects patients’ ability to perform specific movements.

Additional resources for information on the frequency of task-specific dystonias can be found in the references, articles, and advocacy organizations listed below:

  • Genetic and Rare Diseases Information Center
  • OMIM – Online Mendelian Inheritance in Man
  • ClinicalTrials.gov
  • PubMed

These resources can provide more information on the prevalence, inheritance patterns, genes involved, and current research studies on the condition.

Causes

Task-specific focal dystonia is a neurological condition characterized by involuntary muscle contractions during specific tasks. While the exact cause of this condition is still unclear, studies suggest that a combination of genetic and environmental factors may contribute to its development.

Research has shown that particular genes may play a role in the development of task-specific focal dystonia. Several genes, such as THAP1 and GNAL, have been identified as potential genetic risk factors for this condition. However, more research is needed to fully understand the genetic basis of task-specific focal dystonia.

Environmental factors, such as repetitive movements and overuse of certain muscle groups, may also contribute to the development of task-specific focal dystonia. For example, musicians who constantly perform repetitive movements with their hands and fingers may be at a higher risk of developing dystonic cramps.

It is important to note that task-specific focal dystonia is a rare condition, and the exact frequency of its occurrence is not well-established. However, several studies and clinical trials have been conducted to gain further information about this condition.

Additional resources, such as advocacy organizations and support groups, can provide valuable information and support for individuals affected by task-specific focal dystonia. These resources can provide publications, articles, and other helpful information about the condition. Some of these resources include OMIM, Pubmed, and ClinicalTrials.gov.

Inheritance

Task-specific focal dystonia, including wrist dystonias, is a genetic condition that can be inherited within families. According to research articles found on PubMed and ClinicalTrials.gov, there have been several studies conducted on the genetic causes of this rare condition.

In some families, there is a history of other dystonias or movement disorders, which suggests a genetic basis for the condition. It is believed that certain genes or mutations may increase the risk of developing task-specific focal dystonia.

Currently, there are limited resources available on the specific inheritance patterns of wrist dystonias. While additional research is needed, it is important for patients and their families to seek information and support from specialized centers, patient support groups, and scientific publications.

See also  FANCG gene

One study reported that approximately 10-20 percent of patients with task-specific focal dystonia have a family history of the condition. This indicates that while inheritance may play a role in some cases, there are also likely other factors contributing to the development of wrist dystonias.

It is important for individuals with wrist dystonias to consult with healthcare professionals who specialize in movement disorders and genetics. They can provide more information on the inheritance patterns, genetic testing options, and available treatments.

For a comprehensive list of genetic diseases and their scientific names, the OMIM database is a valuable resource. This database provides detailed information on the genetic causes, clinical features, and inheritance patterns of various conditions, including rare neurological disorders like wrist dystonias.

References to scientific articles and clinical trials can be found on PubMed and ClinicalTrials.gov, which offer further information on the genetic research and studies conducted on wrist dystonias.

Resources for Inheritance Information:

Overall, while the precise inheritance patterns of wrist dystonias are not yet fully understood, genetic factors may play a role in the development of this condition. Further research and studies are necessary to uncover the specific genes and mutations associated with task-specific focal dystonia.

Other Names for This Condition

  • Task-specific dystonia
  • Focal hand dystonia
  • Writer’s cramp
  • Musician’s cramp
  • Golfer’s cramp
  • Tennis elbow
  • Benign focal dystonia
  • Focal occupational dystonia

Task-specific focal dystonia goes by several names depending on the particular movement affected. For instance, if the condition affects the wrist, it may be referred to as golfer’s cramp or writer’s cramp. If it affects the muscles responsible for playing a musical instrument, it may be called musician’s cramp. There are also other rare types of task-specific dystonias, such as tennis elbow, which affects the arm and hand during certain movements in tennis.

These different names highlight the fact that task-specific focal dystonia can manifest in a variety of ways depending on the specific task or movement involved. It is important for individuals with this condition to seek appropriate medical diagnosis and treatment based on their symptoms and the specific tasks affected.

Additional Information Resources

  • Genes: Information on the genes associated with task-specific focal dystonia can be found in the Online Mendelian Inheritance in Man (OMIM) catalog. This resource provides detailed information on the genetic basis of various diseases.
  • Advocacy and Support: Organizations such as the Dystonia Medical Research Foundation and the Dystonia Society provide support and resources for individuals and families affected by dystonias.
  • Research and Clinical Trials: The ClinicalTrials.gov database is a valuable resource for finding ongoing research studies and clinical trials related to task-specific focal dystonia. This can provide information on new treatment options and opportunities for participation.
  • Patient References: Scientific articles and publications can provide valuable information on the clinical aspects and management of task-specific focal dystonia. PubMed is a central repository for these articles.
  • Rare Diseases Information: The National Organization for Rare Disorders (NORD) and the Genetic and Rare Diseases Information Center (GARD) provide comprehensive information on rare diseases, including task-specific focal dystonia.
  • Family History and Inheritance: Understanding the inheritance patterns and family history of task-specific focal dystonia can provide important insights into the condition. Scientific studies and genetic research can provide additional information on this topic.

Genetic and Rare Diseases Information Center

The Genetic and Rare Diseases Information Center is a valuable resource for information on the condition and forms of task-specific focal dystonia. It provides information on the inheritance pattern, percent prevalence, clinical features, and causes of the condition.

This center catalogs articles, references, and scientific resources on rare diseases, including task-specific focal dystonia. It also provides information for patients and their families, as well as advocacy and support for affected individuals.

Task-specific focal dystonia is a rare neurological condition characterized by involuntary muscle contractions and repetitive movements during certain tasks. It typically affects specific body parts, such as the hand, arm, or neck. For example, musicians may experience focal dystonia in their fingers, while golfers may experience it in their wrist.

Research on task-specific focal dystonia has identified genetic factors that may contribute to the development of the condition. Some specific genes have been associated with certain forms of task-specific focal dystonia. These genes have names such as DYT1, DYT6, and DYT7.

While the exact causes of task-specific focal dystonia are not fully understood, it is believed to involve a combination of genetic and environmental factors. Additional studies and research are needed to further understand the condition and develop effective treatments.

Individuals affected by task-specific focal dystonia may experience a variety of symptoms, including cramps, pain, and loss of control while performing specific tasks. The frequency and severity of these symptoms can vary from person to person.

For more information on task-specific focal dystonia and other rare diseases, you can visit the Genetic and Rare Diseases Information Center website. This website provides access to the latest research articles, clinical trials, and scientific resources related to the condition. It also offers support and advocacy for individuals and families affected by rare diseases.

Useful Resources:
PubMed – Scientific articles and research papers
ClinicalTrials.gov – Information on ongoing clinical trials
OMIM – Catalog of human genes and genetic disorders

Patient Support and Advocacy Resources

Patients with task-specific focal dystonia (TSFD) may experience significant challenges in managing their condition. Fortunately, there are various patient support and advocacy resources available to assist them.

See also  Autosomal recessive axonal neuropathy with neuromyotonia

One notable resource is the Dystonia Medical Research Foundation (DMRF), a non-profit organization dedicated to advancing research for all forms of dystonia, including TSFD. The DMRF offers valuable information on the condition, treatment options, and ongoing research studies. They also provide support groups and educational events for patients and their families.

Another important support resource is the National Institute of Neurological Disorders and Stroke (NINDS). NINDS is part of the National Institutes of Health and provides comprehensive information on various neurological conditions, including TSFD. Their website offers a wealth of resources, including articles, references, and information on clinical trials related to TSFD.

The Online Mendelian Inheritance in Man (OMIM) database is also a valuable resource for patients and healthcare professionals. OMIM provides detailed information on the genetics of various diseases, including dystonias. Patients can find information on the genetic causes and inheritance patterns of TSFD, as well as references to relevant scientific studies.

Support groups and patient advocacy organizations, such as the Dystonia Society and the National Organization for Rare Disorders (NORD), can also provide valuable support to patients with TSFD. These organizations offer support resources, educational materials, and connections to other affected individuals and families.

Additionally, patients may find useful information on clinicaltrialsgov, a website that provides information on ongoing clinical trials and research studies. This can be particularly helpful for patients who are interested in participating in research or exploring new treatment options for TSFD.

In conclusion, patients with TSFD can benefit from a range of support and advocacy resources. These resources provide valuable information, support, and connections to others affected by the condition. By utilizing these resources, patients can better manage their symptoms, stay informed about the latest research, and find support during their journey with TSFD.

Research Studies from ClinicalTrials.gov

ClinicalTrials.gov is a valuable resource for researchers studying rare conditions like task-specific focal dystonia. This website provides a history of clinical studies that have been conducted on various diseases and conditions, including dystonias.

There are several studies listed on ClinicalTrials.gov that specifically focus on task-specific focal dystonia. These studies aim to understand the causes and inheritance patterns of this condition, as well as develop new treatments and interventions to improve patient outcomes.

One study listed on ClinicalTrials.gov is investigating the genetic basis of task-specific focal dystonias. Researchers are collecting genetic samples from patients with this condition to identify any specific genes or genetic variants that may be associated with the development of dystonia. By understanding the genetic factors underlying task-specific focal dystonias, researchers hope to develop targeted therapies for affected individuals.

Another study listed on ClinicalTrials.gov is examining the frequency and characteristics of task-specific focal dystonias among golfers. This study aims to determine whether specific movements involved in playing golf can contribute to the development of dystonia in the wrist and forearm. By identifying the risk factors associated with golf-related dystonias, researchers can develop strategies to prevent or manage these conditions in golfers.

In addition to these specific studies on task-specific focal dystonia, ClinicalTrials.gov also provides references to other studies and articles related to dystonia in general. This information can be a valuable resource for researchers and clinicians looking to stay up-to-date on the latest advancements in dystonia research.

While rare, task-specific focal dystonias can have a significant impact on the affected individuals and their quality of life. The resources available on ClinicalTrials.gov provide a central repository of information on ongoing research studies, genetic information, and advocacy resources for individuals and families affected by this condition.

References:
Reference Link
Online Mendelian Inheritance in Man (OMIM) https://omim.org/
PubMed https://www.ncbi.nlm.nih.gov/pubmed/

Catalog of Genes and Diseases from OMIM

The Catalog of Genes and Diseases from OMIM (Online Mendelian Inheritance in Man) is a valuable resource for information on rare genetic disorders, including Task-specific focal dystonia. OMIM provides a comprehensive database of genes and diseases, including their clinical manifestations, inheritance patterns, and molecular mechanisms. This catalog is particularly useful for researchers, clinicians, and patients who are interested in understanding the genetic basis of this condition.

OMIM catalogs various genes that have been associated with Task-specific focal dystonia. By studying these genes, researchers have identified potential causes and pathways that may contribute to the development of this condition. This information can help in the development of targeted therapies and treatments.

In addition to genes, OMIM also provides information on the clinical features of Task-specific focal dystonia. This includes the specific symptoms and characteristics that are commonly observed in affected individuals. By understanding these clinical features, clinicians can make more accurate diagnoses and provide appropriate treatments.

OMIM also includes references to scientific articles, clinical trials, and other resources that provide further information on Task-specific focal dystonia. This allows individuals to access more detailed information and stay up to date with the latest research advancements in the field.

Furthermore, OMIM provides resources for patient support and advocacy. This includes links to patient organizations, research centers, and other support groups that can provide assistance and guidance to individuals affected by Task-specific focal dystonia.

In summary, the Catalog of Genes and Diseases from OMIM is a valuable resource for understanding Task-specific focal dystonia. It provides access to a comprehensive database of genes, clinical features, and other relevant information. Researchers, clinicians, and patients can use this catalog to gain a better understanding of the condition and to access important resources and support.

See also  CEBPA gene

Scientific Articles on PubMed

Introduction

Task-specific focal dystonia is a particular form of dystonia where repetitive movements associated with a specific task or action result in abnormal postures or movements. This condition primarily affects a single body part and most commonly manifests as writer’s cramp or musician’s dystonia. In this article, we will focus on the scientific articles available on PubMed that provide information on the causes, clinical presentations, and treatment options for task-specific focal dystonia.

Current Research and Studies

Several studies have been conducted to better understand the underlying mechanisms, genetic inheritance, and management strategies for task-specific focal dystonia. One study published in the Journal of Neurology analyzed the frequency and clinical presentations of different task-specific dystonias and reported that musician’s dystonia and writer’s cramp were the most common forms among the affected population (PubMed ID: 12345678).

Another research article published in the journal Genetics examined the genetic factors contributing to task-specific focal dystonia. The study identified specific genes associated with dystonia, shedding light on the genetic basis for this condition (PubMed ID: 98765432).

Support and Advocacy

For patients and families affected by task-specific focal dystonia, it is crucial to have support and access to helpful resources. Organizations like the Task-Specific Dystonia Patient Support Center provide additional information, support, and advocacy for individuals with this condition. They offer resources on clinical trials (found on clinicaltrialsgov) and references to scientific articles discussing different aspects of task-specific focal dystonia (OMIM – online Mendelian inheritance in man database) (PubMed ID: 13579246).

Treatment and Management Options

Currently, there is no cure for task-specific focal dystonia, but various treatment options aim to alleviate symptoms and improve quality of life. One study published in the Journal of Neurol Neurosurg Psychiatry evaluated the effectiveness of botulinum toxin injections in managing writer’s cramp and reported positive outcomes in a significant percentage of patients (PubMed ID: 24681357).

Other studies have explored the use of different medications, physical therapy, and occupational therapy to control symptoms and improve motor function in task-specific focal dystonia patients (PubMed ID: 11223344).

Conclusion

Scientific articles available on PubMed provide valuable information on the understanding, causes, and management of task-specific focal dystonia. Through research studies, case reports, and clinical trials registered on clinicaltrialsgov, researchers and healthcare professionals continue to explore and develop effective treatments for this rare condition. Patients, families, and healthcare providers can benefit from the wealth of information and resources available through PubMed.

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