The 20 Best Dysfibrinogenemia Doctors Near Me in vernon, CT

Find the Top Dysfibrinogenemia Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 7 doctor with experience in Dysfibrinogenemia near vernon, CT. Of these, 7 are Experienced.

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7 providers found
    Experienced in Dysfibrinogenemia
    Cardiology | Cardiac Electrophysiology | Interventional Cardiology
    Experienced in Dysfibrinogenemia
    Cardiology | Cardiac Electrophysiology | Interventional Cardiology
    Referral may be required

    Chandra K Sacheti MD LLC

    561 Talcottville Rd, 
    Vernon, CT 
     (2.4 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Dushyant Gandhi is a Cardiologist and a Cardiac Electrophysiologist practicing medicine in Vernon, Connecticut. Dr. Gandhi is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, Hypertension, and Familial Neurocardiogenic Syncope. Dr. Gandhi is board certified in American Board Of Internal Medicine, Cardiology, Cardiovascular Disease. Dr. Gandhi is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Family Medicine
    Experienced in Dysfibrinogenemia
    Family Medicine

    Asylum Hill Family Medicine Center Inc

    99 Woodland St, 
    Hartford, CT 
     (11.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Hugh Blumenfeld is a primary care provider, practicing in Family Medicine in Hartford, Connecticut. Dr. Blumenfeld is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. His clinical expertise encompasses Post-Traumatic Stress Disorder (PTSD), Familial Hypertension, Glucocorticoid-Remediable Aldosteronism, and Hypertension. Dr. Blumenfeld is board certified in American Board Of Family Medicine. Dr. Blumenfeld is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Internal Medicine
    Experienced in Dysfibrinogenemia
    Internal Medicine

    Tolland Primary Care

    384 Merrow Rd Ste J, 
    Tolland, CT 
     (7.6 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Gerald Bayona is a primary care provider, practicing in Internal Medicine in Tolland, Connecticut. Dr. Bayona is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 16 other conditions, according to our data. His clinical expertise encompasses High Cholesterol, Chronic Kidney Disease, Hypothyroidism, and Glucocorticoid-Remediable Aldosteronism. Dr. Bayona is board certified in American Board Of Internal Medicine.

    Learn about our expert tiers
    Experienced in Dysfibrinogenemia
    Experienced in Dysfibrinogenemia
    Referral may be required

    Office

    703 Hebron Ave Ste 805, 
    Glastonbury, CT 
     (8.3 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Steven Horowitz is a Cardiologist practicing medicine in Glastonbury, Connecticut. Dr. Horowitz is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. His clinical expertise encompasses Heart Failure, Pulmonary Edema, Heart Failure with Preserved Ejection Fraction (HFpEF), and Heart Attack. Dr. Horowitz is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Internal Medicine
    Experienced in Dysfibrinogenemia
    Internal Medicine

    Trinity Health Of New England Medical Group

    Adult Primary Clinic, 1000 Asylum Ave Ste 1004, 
    Hartford, CT 
     (12.0 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Orlando Torres is a primary care provider, practicing in Internal Medicine in Hartford, Connecticut. Dr. Torres is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Asthma in Children, Asthma, Grass Allergy, and Type 2 Diabetes (T2D). Dr. Torres is board certified in American Board Of Internal Medicine. Dr. Torres is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Internal Medicine
    Experienced in Dysfibrinogenemia
    Internal Medicine

    Connecticut Surgical Group PC

    1260 Silas Deane Hwy, 
    Wethersfield, CT 
     (12.8 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    Sakshi Kapur is a primary care provider, practicing in Internal Medicine in Wethersfield, Connecticut. Dr. Kapur is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. She is also highly rated in 40 other conditions, according to our data. Her clinical expertise encompasses Anemia, Childhood Iron Deficiency Anemia, Myelodysplastic Syndrome (MDS), Hernia Surgery, and Pacemaker Implantation.

    Experienced in Dysfibrinogenemia
    Family Medicine
    Experienced in Dysfibrinogenemia
    Family Medicine

    Hartford Healthcare Medical Group

    336 North Main St, 
    West Hartford, CT 
     (14.8 miles away)
    Languages Spoken:
    English

    Batel Isenstein is a primary care provider, practicing in Family Medicine in West Hartford, Connecticut. Dr. Isenstein is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. Her clinical expertise encompasses High Cholesterol, Hypothyroidism, Multiple Endocrine Neoplasia Type 1, and Familial Hypertension.

    Showing 1-7 of 7

    Last Updated: 09/26/2026

    What is the definition of Dysfibrinogenemia?

    Dysfibrinogenemia is a coagulation (clotting) disorder characterized by having an abnormal form of fibrinogen. Fibrinogen is a protein produced by the liver which helps control bleeding by helping blood clots to form. Having abnormal fibrinogen results in defective clot formation and can cause an increased or decreased ability to clot. Dysfibrinogenemias may be inherited (congenital) or acquired. Congenital Dysfibrinogenemia is rare. About 40% of people with this form have no symptoms. About 50% have a bleeding disorder, and the remaining 10% have either a thrombotic disorder (excessive clotting) or both bleeding and thrombotic disorders. Congenital Dysfibrinogenemias may be caused by genetic changes in the FGA, FGB or FGG genes. Inheritance is most often autosomal dominant or codominant, but can also be autosomal recessive. Whether a person has no symptoms, a bleeding tendency, or an increased risk of thrombosis depends on the effect of their specific genetic change(s). Acquired Dysfibrinogenemia is more common than the congenital form and is associated with liver disease such as cirrhosis, liver tumors, or hepatitis.