What is Dentatorubral Pallidoluysian Atrophy?

What is Dentatorubral Pallidoluysian Atrophy?

• Dentatorubral Pallidoluysian Atrophy: A condition caused by an abnormality of the DNA sequence on chromosome 12.

Dentatorubral Pallidoluysian Atrophy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Dentatorubral Pallidoluysian Atrophy, or a subtype of Dentatorubral Pallidoluysian Atrophy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Dentatorubral Pallidoluysian Atrophy as a "rare disease".
Source - Orphanet

Dentatorubral Pallidoluysian Atrophy: Introduction

Types of Dentatorubral Pallidoluysian Atrophy:

Broader types of Dentatorubral Pallidoluysian Atrophy:

• Triplet Repeat Genetic Disorders
• more types...»

How serious is Dentatorubral Pallidoluysian Atrophy?

Complications of Dentatorubral Pallidoluysian Atrophy: see complications of Dentatorubral Pallidoluysian Atrophy

What causes Dentatorubral Pallidoluysian Atrophy?

Causes of Dentatorubral Pallidoluysian Atrophy: see causes of Dentatorubral Pallidoluysian Atrophy

What are the symptoms of Dentatorubral Pallidoluysian Atrophy?

Symptoms of Dentatorubral Pallidoluysian Atrophy: see symptoms of Dentatorubral Pallidoluysian Atrophy

Complications of Dentatorubral Pallidoluysian Atrophy: see complications of Dentatorubral Pallidoluysian Atrophy

Can anyone else get Dentatorubral Pallidoluysian Atrophy?

Inheritance of genetic conditions: see details in inheritance of genetic diseases.

Dentatorubral Pallidoluysian Atrophy: Testing

Diagnostic testing: see tests for Dentatorubral Pallidoluysian Atrophy.

Misdiagnosis: see misdiagnosis and Dentatorubral Pallidoluysian Atrophy.

How is it treated?

Treatments for Dentatorubral Pallidoluysian Atrophy: see treatments for Dentatorubral Pallidoluysian Atrophy

Name and Aliases of Dentatorubral Pallidoluysian Atrophy

Main name of condition: Dentatorubral Pallidoluysian Atrophy

Class of Condition for Dentatorubral Pallidoluysian Atrophy: genetic repeating triplet

myoclonic epilepsy with choreoathetosis, Naito-Oyanagi disease, DRPLA, NOD

DRPLA, Myoclonic epilepsy with choreoathetosis, NOD, Naito Oyanagi disease
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Research the causes of these diseases that are similar to, or related to, Dentatorubral Pallidoluysian Atrophy:

• Spinocerebellar ataxia
• Dysarthria
• Dysphagia
• Ataxia
• Olivopontocerebellar atrophy
• Multiple system atrophy
• MSA
• Autosomal dominant cerebellar atrophy
• Spinocerebellar atrophy
• ADCA
• Menzel OPCA
• Menzel ataxia

Rate This Website

What do you think about the features of this website? Take our user survey and have your say:

Website User Survey

Medical Tools & Articles:

Next articles:

• Online Medical Textbooks for Dentatorubral Pallidoluysian Atrophy
• Prevalence and Incidence of Dentatorubral Pallidoluysian Atrophy
• Videos related to Dentatorubral Pallidoluysian Atrophy
• Causes of Dentatorubral Pallidoluysian Atrophy
• Symptoms of Dentatorubral Pallidoluysian Atrophy

Tools & Services:

• Bookmark this page
• Take a survey relating to Dentatorubral Pallidoluysian Atrophy
• Symptom Search
• Symptom Checker
• Medical Dictionary
• Give your feedback

Medical Articles:

• Disease & Treatments Search
• Misdiagnosis Center
• Full list of interesting articles

Forums & Message Boards

• Ask or answer a question at the Boards:
• I cannot get a diagnosis. Please help.
• Tell us your medical story.
• Share your misdiagnosis story.
• What is the best treatment for my condition?
• See all the Boards.

Enter your search terms Submit search form
Search The Web Search wrongdiagnosis.com

Common Health Mistakes

Symptom
Checker

Search Specialists by State and City