The 20 Best Dysfibrinogenemia Doctors Near Me in laurinburg, NC

Find the Top Dysfibrinogenemia Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Dysfibrinogenemia near laurinburg, NC. Of these, 1 are Experienced.

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1 provider found
    Experienced in Dysfibrinogenemia

    Dr. Sejal Dave
    Hematology Oncology | Hematology | Oncology
    Experienced in Dysfibrinogenemia

    Dr. Sejal Dave
    Hematology Oncology | Hematology | Oncology
    Referral may be required

    Scotland Cancer Treatment Center (Duke Cancer Network)

    500 Lauchwood Dr, 
    Laurinburg, NC 
     (1.6 miles away)
    910-291-7630
    Languages Spoken:
    English, Arabic, Hebrew, Hindi
    See accepted insurances
    Accepting New Patients
    Offers Telehealth

    Sejal Dave is a Hematologist Oncology specialist and a Hematologist practicing medicine in Laurinburg, North Carolina. Dr. Dave is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Familial Colorectal Cancer, Colorectal Cancer, Paget Disease of the Breast, and Childhood Iron Deficiency Anemia. Dr. Dave is board certified in American Board Of Internal Med, Hematology and American Board Of Internal Med, Medical Oncology. Dr. Dave is currently accepting new patients.

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    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.

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