Top Tweets for #sequencemd
Did you know your DNA affects how medications work in your body? Pharmacogenomics helps doctors match the right drug and dose to your unique genetic profile.
Learn more: https://t.co/aJ3mFPce8U
#pharmacogenomics #DNAtesting #adultgenetics #SequenceMD
Up to 40% of adult epilepsy cases have a genetic component — but most people never get evaluated. A genetic diagnosis can guide better treatment decisions and open doors to emerging therapies. Learn more: https://t.co/gIHEvD6gEv
#sequencemd #genetictesting #adultepilepsy
Polygenic Risk Scoring analyzes 100s of variants to estimate your likelihood of developing heart disease, Alzheimer’s, cancer and more. Combined with lifestyle + family history, it becomes a powerful prevention tool: https://t.co/rTtnHZKArG
#SequenceMD #PRS #GeneticRisk
Your genes influence how medications work. PGx testing helps personalize treatment, avoid side effects and find the right medication faster. LEARN MORE: https://t.co/QOHOsrTK1F
#PGx #PersonalizedMedicine #SequenceMD #medication
Genetic testing is unlocking answers in kidney disease — clearer diagnoses, tailored treatment, early risk detection and more. See how genetics supports long-term kidney health here: https://t.co/x0U5xFlqIn
#genetictesting #sequencemd #diagnosis #raredisorders #kidneydisease
Fabry disease and nephronophthisis (NPHP) are rare genetic disorders that affect the kidneys. Genetic testing can confirm a diagnosis, identify gene mutations, and guide understanding of disease progression and treatment options.
#genetictesting #sequencemd #fabrydisease #NPHP
Alport syndrome is a rare genetic condition that affects kidneys, hearing and vision. Genetic testing can confirm a diagnosis, guide care and help assess the risk of complications.
Learn more: https://t.co/x0U5xFlqIn
#genetictesting #sequencemd #raredisorders #alportsyndrome
Your DNA can impact kidney disease. PKD causes cysts in the kidneys that may lead to failure. Genetic testing helps guide more personalized care. More info: https://t.co/x0U5xFlqIn
#genetictesting #kidneydisease #sequencemd
Unravel the genetic puzzle of kidney disease: Your DNA can influence your risk. Learn how genetics affect kidney health and common inherited conditions. Spoiler: 60+ genetic kidney diseases play a major role in young patients: https://t.co/x0U5xFlqIn
#sequencemd #kidneydisease
Inherited eye disorders can cause vision loss, blindness, or other challenges — and genetics may hold the answers. Explore the types, symptoms and treatments in our blog:
https://t.co/kzibY9ua3z
#genetictesting #eyehealth #visioncare #sequencemd #eyedisorders #visionloss
Exploring your genetics? You’ve likely seen screening vs. diagnostic testing. Screening spots risks, diagnostics confirm + guide care. Both matter for your health journey. Learn more via our recent blog: https://t.co/wve3NdNkAW
#SequenceMD #GeneticScreening #DiagnosticTesting
Carrier screening can uncover hidden risks for inherited conditions like CF, SMA, or fragile X. SequenceMD offers expert counseling + evidence-based panels so you can make informed choices when starting a family.
#CarrierScreening #GeneticsTesting #SequenceMD
Cardiomyopathy diseases can weaken, thicken or stiffen the heart, causing shortness of breath, fatigue, swollen legs or feet, chest pain, and irregular heartbeats. Early detection is key to managing the condition: https://t.co/33z5iI77NM
#sequencemd #genetics #heartcondition
Do you have family members with cardiac issues? Even if people in your family received a diagnosis, it’s possible they haven’t been checked to determine whether something heredity is the cause. LEARN MORE: https://t.co/hT01vgSVXI
#sequencemd #genetics #cardiaccondition
RESEARCH AND CLINICAL TRIALS: Children who receive a genetic diagnosis can be eligible to participate in studies investigating the disease effects, course and management. LEARN MORE: https://t.co/WUELUKv01K
#sequencemd #geneticresearch #genetictrials #childhoodgenetics
PERSONALIZED CARE FOR GENETIC DISEASES IN CHILDREN: Treatments for genetic disorders are continually improving and expanding. By 2025, the FDA may approve 10 to 20 new gene and cell therapies yearly.
READ MORE: https://t.co/WUELUKv01K
#sequencemd #genetictesting #genetherapy
TRACKING AND MONITORING YOUR CHILD’S DISEASE: After knowing the diagnosis, doctors can monitor symptoms and proactively plan for and manage progression and complications. READ MORE: https://t.co/WUELUKv01K
#sequencemd #genetictesting #genetics #caremanagement #raredisorders
EDUCATED DECISION-MAKING: A diagnosis will assist you in making well-informed choices regarding your child's care. It lets you plan and avoid any stressors that aggravate or cause symptoms.
LEARN MORE >>> https://t.co/WUELUKv01K
#sequencemd #genetics #genetictesting
A rare genetic condition diagnosis for a child takes time and money without the support of genetic testing. Genetic diagnoses let families and clinicians focus on what matters. Learn more here: https://t.co/WUELUKvxRi
#sequencemd #raregeneticdisorders #childgenetictesting
9. Research Patient Resources: If you believe your doctor isn’t listening, find patient advocate resources. The Patient Advocate Foundation (https://t.co/nnOq98A4zY) is a well-known one.
Other ways to lobby for health care: https://t.co/ulQMjQ8AZc
#sequencemd #patientadvocacy
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