SequenceMD provides medical genetics services within community health systems to adults and families with rare conditions, unique, or unmet medical needs
There are 4 areas where genetics can make a real difference for patients. #1 is managing medications when scientists study how our genetic makeup affects our response to medication. Learn where adult genetics matter most: https://t.co/aJ3mFPce8U
#adultgenetics#geneticstesting
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
Unexplained muscle weakness in a patient under 50? Symmetrical? No inflammation on labs?
Those are red flags for a neurogenetic cause — and a signal that whole genome sequencing should happen. Learn how we evaluate and manage genetic muscle weakness: https://t.co/JM9aXZBVjm
Happy National Doctors’ Day to the physicians who never stop asking why. At SequenceMD, we have the privilege of partnering to unravel unresolved symptoms, undiagnosed conditions, and complex genetic and metabolic diagnoses for patients of all ages.
#RareDiseases#GeneticTesting
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
On Rare Disease Day (that’s today!), we stand with those searching for answers. Millions remain undiagnosed. SequenceMD works to shorten the journey — because every patient deserves clarity, care and hope.
Learn more: https://t.co/784MWD4qql.
#GeneticCounseling#RareDiseaseDay
Doctors are taught when they “hear hoofbeats,” to expect a horse, not a zebra. In the rare disease community, one in 10 Americans is a zebra. SequenceMD helps find answers through genetic testing: https://t.co/Nm2iKIraQp
#RareDiseaseDay#GeneticTesting#ShowYourStripes
This Rare Disease Day (Feb. 28), stand with the rare disease community. At SequenceMD, we help families with diagnostic clarity through genetic evaluations and counseling. Learn four key areas where genetics matters most in primary care: https://t.co/g6xCLACY2j
#RareDiseaseDay
Rare Disease Day (Feb. 28) raises awareness and support for everyone on a rare medical journey. Through comprehensive genetic evaluations, SequenceMD helps patients understand what a diagnosis means — and next steps. Learn more: https://t.co/784MWD4qql
#RareDiseaseDay#Genetics
Rare Disease Day (Feb. 28) is about action. There are 10,000+ rare diseases and fewer than 5% have approved treatments. If you have unexplained health issues, genetic testing with SequenceMD may help find answers. Learn more: https://t.co/yl3DbhMMyo
#RareDisease#Genetics
Not knowing can be the hardest part of a rare disease journey. SequenceMD helps uncover genetic answers — so you can move forward with clarity.
Could genetics testing help you? Read “10 Red Flags You May Have a Genetic Disease”: https://t.co/WJNLbqLahV
#RareDiseaseDay#Genetics
Rare Disease Day (Feb 28) shines a light on the 300M+ people worldwide living with a rare disease. At SequenceMD, we help patients pursue answers via genetic testing and counseling. Learn more: https://t.co/Qp5t9UzpER
#RareDiseaseDay#GeneticCounseling#ShowYourStripes
SequenceMD serves three key groups affected by genetic neurodevelopmental disorders (NDDs): newly diagnosed children and young adults, kids facing long waits for testing, and adults with IDD who’ve never had a genetic evaluation. Learn more here: https://t.co/m3dYCtTIcd
#NDD
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
Welcome Lucy Holt, SequenceMD’s newest genetic counselor! With experience in oncology/hematology genetics and gene-therapy research, she supports patients through cancer risk and rare disease evaluations. For her full bio: https://t.co/fSicz26GMK
#genetics#rarediseases
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