Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 

GM1 gangliosidosis

GM1 gangliosidosis: Introduction

GM1 gangliosidosis: A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type 1 is a severe infantile form of the disorder and involves a greater degree of accumulation than type II or III. More detailed information about the symptoms, causes, and treatments of GM1 gangliosidosis is available below.

Symptoms of GM1 gangliosidosis

Home Diagnostic Testing

Home medical testing related to GM1 gangliosidosis:

Wrongly Diagnosed with GM1 gangliosidosis?

GM1 gangliosidosis: Deaths

Read more about Deaths and GM1 gangliosidosis.

Causes of GM1 gangliosidosis

Read more about causes of GM1 gangliosidosis.

GM1 gangliosidosis: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and GM1 gangliosidosis

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 multiple sclerosis). See symptoms of...read more »

GM1 gangliosidosis: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for GM1 gangliosidosis

Medical research articles related to GM1 gangliosidosis include:

Click here to find more evidence-based articles on the TRIP Database

Research about GM1 gangliosidosis

Visit our research pages for current research about GM1 gangliosidosis treatments.

Statistics for GM1 gangliosidosis

GM1 gangliosidosis: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about GM1 gangliosidosis, or answer someone else's question, on our message boards:

Definitions of GM1 gangliosidosis:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list GM1 gangliosidosis as a "rare disease".
Source - Orphanet

Related GM1 gangliosidosis Info

Videos about GM1 gangliosidosis

 

More information about GM1 gangliosidosis

  1. GM1 gangliosidosis: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Deaths
 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise