GNE Myopathy, also known as Hereditary Inclusion Body Myopathy (HIBM), is a rare inherited disease that causes severe muscle weakness in the legs and arms, usually leading to physical disability within twenty years of onset. Although, some patients are able to live using just a cane for many years, in most patients the quadriceps muscles are spared. GNE Myopathy does not affect the vital organs such as the heart, the lungs and the swallowing ability.
The disease is found in many populations worldwide: Europeans, South Americans, Africans, Middle Easterns; Arabs, Jews, Persians, and Asians of Japanese and Indian descent among others.
For a more comprehensive description on GNE Myopathy please refer to the National Institutes of Health, devoted to educating patients, families and doctors.
Here is a link to a short video explaining GNE Myopathy
What Causes GNE Myopathy/HIBM?
GNE Myopathy is believed to be caused by a genetic mutation. The GNE gene encodes an enzyme that is responsible for producing sialic acid, an important component in muscle function. The body’s failure to produce and maintain sufficient sialic acid levels causes muscles to slowly weaken.
What are Some of the Symptoms?
Symptoms of the disease typically begin between the ages of 20 and 35, but in some cases it is even later. Below is a list of common symptoms:
Difficulty in climbing stairs
Difficulty in getting up from a seated position
Difficulty in running
Loss of balance
Weakness in index fingers
Weakness in arms and shoulder
If you have some of these symptoms and would like to have an online diagnosis check the ALDA free diagnostic tool. (Note: this is not a substitute for seeing a physician, but can set you on the right path)
When is a Good Time to Get Tested?
If you experience any of the symptoms listed above, and have family members already affected with GNE Myopathy, you should get tested by medical specialists. A list of International doctors familiar with GNE Myopathy.
Where can I be tested?
Your doctor should be able to preform a proper test for you, but in the event that this is not possible, please refer to the below resources:
UCLA Genetic Dept., Dr. Wayne Grody, M.D., Ph.D. 10833 Le Conte Ave. #12138
Los Angeles, CA 90095
Appointments: (310) 825-0867
Information: (310) 206-6581
San Fransisco Bay Area
Open Medicine Institute
2500 Hospital Drive. Building #2
Mountain View, CA 94040
Ask O.M.I. about how to schedule an in-home screening and/or scheduled screenings anywhere in the U.S.
What are Some Other Names by Which GNE Myopathy is Known?
It is officially now known as GNE Myopathy, which has been named after the affected gene. Previously, it was widely known as HIBM (Hereditary Inclusion Body Myopathy), but it has also been known as:
DMRV – Distal Myopathy with Rimmed Vacuoles
QSM – Quadriceps Sparing Myopathy
HIBM2 – Hereditary Inclusion Body Myopathy-Type 2
IBM2 – Inclusion Body Myopathy-Type 2
What if You Have Been Recently Diagnosed?
If you have been recently diagnosed with GNE Myopathy, also known as HIBM, you may be overwhelmed and afraid; but fortunately you are not alone. NDF is the world's largest organization focused on GNE Myopathy and we are here for you. Please see our list of resources for other groups and organizations that may also be helpful to you in different parts of the world.
Currently, there are clinical trials in which you may want to consider participating, such as those conducted by the National Institutes of Health (NIH). In addition, many resources exist that can offer you and/or your family the support that you need.
How Do I Know if I am a Carrier?
GNE Myopathy is an autosomal recessive disorder, which means that the parents of someone affected by GNE Myopathy are carriers of the disease. Carriers are not affected by the disease, which means that their bodies function normally. But when two carriers have a child, there is a 25% chance with each pregnancy of having a child who actually has GNE Myopathy, there is a 50% chance that each child will be a carrier like his or her parents (and not have the disease), and there is a 25% chance that each child of the couple will not carry any mutation for the disease (meaning that he or she will not be a carrier nor will he or she have the disease).
It is possible to be tested at any time, but it is particularly important prior to becoming pregnant or during early pregnancy.
Testing is anonymous and can be performed with a painless cheek swab.
Is There a Treatment or Cure?
What is a Patient Registry?
A patient registry collects information on patients with GNE Myopathy. The information is stored in a database and is made available to researchers who are studying this disease.
Please register to become a part of this database at:
What is a Natural History Study?
Natural history studies allow scientists to collect anonymous data from patients from all over the world to gain a better understanding of GNEM. They track progression over time and identify demographic, genetic and environmental variables that correlate with a specific disease. Even if you do not want personal information used, this is an anonymous way to contribute to advancing the general understanding of GNEM.
To participate in this you will need to travel to a hospital that conducts the natural history studies. Researchers want to learn more about the causes, symptoms, and effects of GNE Myopathy. Your medical and genetic information will be collected as well as muscle tests, blood samples and other tests as needed.
What if I want to start a family, and I am a Carrier?
Read more on inheritance patterns here.
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Click the image below for a detailed and comprehensive explanation of GNEM (HIBM)
Please feel free to download and share with your doctor(s)