Limb-Girdle Muscular Dystrophy Type 2E
Are you a genetic carrier for Limb-Girdle Muscular Dystrophy? Find out with this DNA Test.
- Detects the most common SGCB variant linked to limb-girdle muscular dystrophy type 2E
- Carrier screening test intended for couples who are planning to become pregnant
- Determine the risk of your child inheriting this condition that affects muscle strenght
- 100% private and confidential online results
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Limb-girdle muscular dystrophies are a group of inherited diseases that leads to weakness and atrophy (wasting) of the muscles. The bone structures that surround the shoulder area (shoulder girdle) and the bone structures that surround the hips (pelvic girdle) are collectively referred to as the limb girdles. Limb-girdle muscular dystrophy affects the proximal muscles (muscles closest to the center of the body) around the hips and shoulders.
Limb-girdle muscular dystrophy type 2E (LGMD2E) is the most common type of limb-girdle dystrophy in people of Southern Indiana Amish descent. It is caused by genetic variation in the SGCB gene, which provides instructions to produce a component (subunit) of the sarcoglycan protein complex. Genetic variants of SGCB affect either the formation of the sarcoglycan complex and/or its function, leading to the characteristic features of muscle weakness observed in limb-girdle muscle dystrophy.
Take this test to find out whether you are a genetic carrier of the SGCB variant and are at risk of passing it to your children. This is intended to be a carrier screening test for couples who are considering to start a family.
Limb-girdle muscular dystrophy type 2E is caused by genetic variation in the SGCB gene, which provides instructions to produce a component (subunit) of the sarcoglycan protein complex. In affected people the production of the sarcoglycan protein complex is disrupted giving rise to symptoms associated with LGMD2E.
This condition is inherited in an autosomal recessive pattern, which means two defective copies of the SGCB gene must be inherited in order for the disease to manifest.
This test looks at one variant of SGCB linked to limb-girdle muscular dystrophy type 2E that occurs approximately in 99% of the carriers of Amish descent.
- rs28936383 C (T151R)
Understanding your carrier status for these variants will help you understand the risk of passing it to your children.
While it provides a risk analysis for limb-girdle muscular dystrophy type 2E, complete genome sequence analyses may be necessary to identify additional variants associated with other subtypes of limb-girdle muscular dystrophy.
Signs & Symptoms
Following signs and symptoms usually develop in affected infants and children
- Progressive muscle weakness, particularly arm and leg muscles nearest the torso
- Heart problems
- Lung problems
- Spine curve
- Changes in posture or in the appearance of shoulder, back and arm muscles
- Scapular winging
- Abnormal curving in their lower back (lordosis)
- Joint stiffness
- Reduced lifespan
How It Works
Step 1: Sign up for a free Genebase account.
Step 2: Upload your DNA markers to Genebase.
Step 3: Login to your account to access your results when they are ready.