Sclerosteosis Blood Test

What is Sclerosteosis?

Sclerosteosis is an extremely rare genetic disorder characterized by excessive bone growth throughout the body, leading to increased bone density and nerve compression. It is caused by mutations in the LRP4 gene, which regulates bone formation by controlling the Wnt signaling pathway. The MuSK and LRP4 Antibodies Panel is the most important test for detecting abnormal LRP4 protein function that may warrant genetic testing for this rare bone disorder.

RECOMMENDED TEST MuSK and LRP4 Antibodies Panel
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What causes sclerosteosis?

Sclerosteosis is caused by mutations in the LRP4 gene, which plays a critical role in regulating bone formation through the Wnt signaling pathway. These genetic mutations disrupt the normal process that controls bone growth, leading to excessive and progressive bone formation throughout the body. The condition is inherited in an autosomal recessive pattern, meaning both parents must carry the mutated gene for a child to develop sclerosteosis.

What is the best test for sclerosteosis?

The MuSK and LRP4 Antibodies Panel is the most important blood test for sclerosteosis because it detects antibodies against LRP4 protein, which is directly affected by the LRP4 gene mutations causing this condition. Abnormal LRP4 antibody levels may indicate disrupted protein function and provide supporting evidence that warrants comprehensive genetic testing. While definitive diagnosis requires DNA sequencing to identify LRP4 gene mutations, this antibody panel serves as a valuable preliminary screening tool that can guide your healthcare provider toward appropriate genetic testing and specialist consultation.

When should I get tested for sclerosteosis?

You should get tested if you have a family history of sclerosteosis or are experiencing symptoms like excessive bone growth, facial asymmetry, hearing loss, or headaches caused by nerve compression. Testing is also recommended if you notice progressive thickening of facial bones, skull enlargement, or if you have had multiple family members with unusually dense bones. Early detection through blood testing can help guide genetic counseling and management strategies before severe complications develop.

What are the symptoms of sclerosteosis?
Sclerosteosis symptoms include progressive facial distortion with a square jaw and prominent forehead, hearing loss due to narrowing of the ear canals, headaches from increased skull pressure, and nerve compression causing pain or paralysis. You might notice unusually tall stature during childhood, syndactyly (fused fingers or toes), and dental problems due to jaw overgrowth. The excessive bone growth typically becomes more apparent during childhood and adolescence as skeletal development progresses.
Who is at risk for sclerosteosis?
Sclerosteosis primarily affects individuals of Afrikaner descent in South Africa, where the condition was first identified and remains most common due to a founder effect. You are at highest risk if both of your parents carry the LRP4 gene mutation, as the condition follows an autosomal recessive inheritance pattern. Genetic counseling is recommended for families with a history of sclerosteosis or individuals from populations where the condition is more prevalent.
What happens if sclerosteosis is left untreated?
Untreated sclerosteosis leads to progressive bone overgrowth that can cause severe complications including permanent hearing loss, facial nerve paralysis, vision problems from optic nerve compression, and increased intracranial pressure leading to chronic headaches. The excessive bone density puts you at risk for life-threatening complications such as brainstem compression, seizures, and respiratory difficulties. Early monitoring and intervention are essential to prevent irreversible nerve damage and maintain quality of life.
Can sclerosteosis be diagnosed with a blood test?
Sclerosteosis cannot be definitively diagnosed with blood tests alone, but the MuSK and LRP4 Antibodies Panel can detect abnormal LRP4 protein function that supports the diagnosis. Blood antibody testing serves as a preliminary screening tool that may indicate the need for comprehensive genetic testing, which remains the gold standard for confirming LRP4 gene mutations. A combination of clinical examination, imaging studies showing increased bone density, and genetic testing provides the most accurate diagnosis.
How is sclerosteosis treated?
Sclerosteosis treatment focuses on managing symptoms and preventing complications through surgical interventions to relieve nerve compression, decompress the skull to reduce intracranial pressure, and address hearing loss with cochlear implants or hearing aids. Your healthcare team may recommend regular monitoring with imaging studies to track bone growth progression, physical therapy to maintain mobility, and pain management strategies. While there is no cure for the genetic condition itself, early intervention can significantly improve quality of life and prevent serious complications.
How can I prevent sclerosteosis?
Sclerosteosis cannot be prevented because it is an inherited genetic disorder caused by mutations in the LRP4 gene. However, genetic counseling and carrier testing before having children can help you understand your risk of passing the condition to your offspring if you have a family history of sclerosteosis. Prenatal genetic testing is available for couples who both carry the LRP4 mutation and want to assess whether their baby will be affected by this rare condition.
What can I do at home for sclerosteosis?
While home remedies cannot treat the underlying genetic cause of sclerosteosis, you can manage symptoms by maintaining regular follow-up appointments with specialists to monitor bone growth and prevent complications. Stay proactive about hearing health by using hearing protection and assistive devices as recommended, practice good oral hygiene to address dental complications, and maintain a healthy lifestyle with appropriate nutrition and exercise within your physical limitations. Connect with support groups for rare bone disorders to share experiences and coping strategies with others who understand the challenges of living with sclerosteosis.
How’s this work?
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Long story short:
  1. In the test options, use the filters or search box to narrow your choices and find the test you want.
  2. If you need a hand navigating through options, text our super friendly support team at 754-799-7833, and we'll provide tailored suggestions to help you find the ideal test.
  3. Once your order is placed, we’ll create your doctor’s lab order remotely, without any need for you to make a trip to a doctor in person or to talk to the doctor. Expect to receive your doctor’s lab order right in your inbox. It will also be in your patient portal if you need to find it later. We’ll also include instructions regarding fasting and other requirements for your test. Your patient portal will be auto-created hassle-free during checkout.
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  5. When you’re ready, visit one of our 4,000 locations. Just bring your ID – no printing or faxing of your lab order is needed, as your order and details will already be in the lab system.
  6. Note that most lab locations don’t accept walk-ins, so it’s best to book an appointment in advance. Don’t worry – we’ll provide detailed instructions along the way.
  7. You’ll get your results via email & SMS and dive into understanding your body better. Yup, that easy!
  8. If you have any questions, please text us at 754-799-7833 or email support@privatemdlabs.com and we'll gladly help you.
How do I know which test to get?
In the test options, find the test you want. If you’re not sure which test to get, we can lend a hand in finding the right option.

Just text or call us at 754-799-7833, email us at support@privatemdlabs.com, and we'll gladly help you. We've got your back and reply quickly.
Is it possible to make changes to my lab order if I made a mistake with the name, date of birth, or any other details?
Absolutely! We totally understand that errors can happen. No worries, we're here to help you.

Just reach out to us via text at 754-799-7833 or shoot us an email at support@privatemdlabs.com. Remember to include your order number and let us know the correct information you’d like to update. Our awesome team will jump right in and make sure everything is sorted out and accurate for you.

There are no changes necessary if your address is wrong on the requisition though. We don’t mail anything out.

Our lab requires an address to be listed to generate an order.
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Only HSA & FSA is accepted.

Our services are strictly self-pay and cannot be submitted to your health insurance provider except for Health Savings Accounts or Flexible Savings Accounts.

This policy applies to all insurance companies, including federal health insurance programs like Medicare.

If you have any questions, please text us at 754-799-7833 or email support@privatemdlabs.com.
Can I cancel my order?
Yes.

We get it – sometimes your needs change.

As long as your samples haven’t been collected yet, we’re happy to help you cancel your order.

If you have any further questions, please text us at 754-799-7833 or email support@privatemdlabs.com.

You can read more about our cancellation policy here.
How can I find a lab location near me?
During the ordering process, you’ll be able to select a specific lab near you, with no strings attached! You can switch it up later easily and visit any of our authorized locations as long as it’s the same lab company you selected your test for (Quest Diagnostics or Labcorp).

Before you proceed with your order, feel free to browse through all our lab locations here. This will give you the peace of mind of knowing that there's a lab nearby your home, office or your favorite gym.

If you have any questions, please text us at 754-799-7833 or email support@privatemdlabs.com and we'll gladly help you.
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MuSK and LRP4 Antibodies Panel
Google reviews 505 reviews
$7,400 $5,772
What's included
Fast & easy, results by email & SMS
No need to visit a doctor
Private & confidential
No insurance needed
Results explained
No extra fees paid at the lab

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