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Erythrokeratodermia ataxia

Erythrokeratodermia ataxia: Introduction

Erythrokeratodermia ataxia: A rare inherited condition characterized by skin and nervous system disorders. More detailed information about the symptoms, causes, and treatments of Erythrokeratodermia ataxia is available below.

Symptoms of Erythrokeratodermia ataxia

Home Diagnostic Testing

Home medical testing related to Erythrokeratodermia ataxia:

Wrongly Diagnosed with Erythrokeratodermia ataxia?

Causes of Erythrokeratodermia ataxia

Read more about causes of Erythrokeratodermia ataxia.

Disease Topics Related To Erythrokeratodermia ataxia

Research the causes of these diseases that are similar to, or related to, Erythrokeratodermia ataxia:

Erythrokeratodermia ataxia: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Erythrokeratodermia ataxia

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is that psoriasis is rare in children, and more »

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of more »

Erythrokeratodermia ataxia: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Erythrokeratodermia ataxia: Animations

Statistics for Erythrokeratodermia ataxia

Erythrokeratodermia ataxia: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Erythrokeratodermia ataxia, or answer someone else's question, on our message boards:

Definitions of Erythrokeratodermia ataxia:

Erythrokeratodermia ataxia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Erythrokeratodermia ataxia, or a subtype of Erythrokeratodermia ataxia, 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 Erythrokeratodermia ataxia as a "rare disease".
Source - Orphanet

Related Erythrokeratodermia ataxia Info

More information about Erythrokeratodermia ataxia

  1. Erythrokeratodermia ataxia: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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