Understanding the Genetic Cause of Your Low Calcium
If you or a loved one are living with chronic low calcium (hypocalcemia), a genetic test can help identify the underlying cause and guide you to the right trajectory of care.
Genetic Testing Program
No-cost genetic testing for ADH1
Autosomal Dominant Hypocalcemia Type 1
Recognizing the Signs of ADH1
ADH1 is a rare genetic condition that affects how the body regulates calcium. Consider genetic testing if you experience:
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Muscle Cramps or Spasms
Frequent twitching or "pins and needles" sensations.
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Seizures
Unexplained episodes related to low calcium levels.
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Kidney Issues
A history of kidney stones or calcification (nephrocalcinosis).
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Family History
Other family members with similar mineral imbalances.
Why Genetic Testing Matters
Knowledge is power for you and your family.
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Precision
Confirm if your hypocalcemia is caused by an ADH1 mutation.
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Family Insight
Help relatives understand their own potential genetic risks.
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Informed Care
Empower your doctor to tailor a management plan specific to your genetic profile.
How the Sponsored Testing Program Works
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Download the Patient Discussion Guide and bring it to your next appointment.
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Your doctor will review your medical history and determine if the test is necessary.
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If approved, your doctor will collect a simple blood or saliva sample.
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Results are typically sent to your doctor within 3–4 weeks to discuss the next steps with you.
Expert guidance, from start to finish
Curious about how sponsored testing works or what your results might mean for your family? Our team of experts is ready to provide the answers and resources you need to move forward with confidence.