The 20 Best Dysfibrinogenemia Doctors Near Me in weirton, WV

Find the Top Dysfibrinogenemia Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 4 doctor with experience in Dysfibrinogenemia near weirton, WV. Of these, 4 are Experienced.

Location
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4 providers found
    Experienced in Dysfibrinogenemia
    Hematology Oncology
    Experienced in Dysfibrinogenemia
    Hematology Oncology
    Referral may be required

    Trinity Tony Teramana Medical Oncology, In Partnership With UPMC Hillman Cancer Center

    3204 Johnson Road, 
    Steubenville, OH 
     (4.0 miles away)
    Languages Spoken:
    English, Arabic, Hindi, Urdu
    Accepting New Patients
    Offers Telehealth

    M Rahman is a Hematologist Oncology provider practicing medicine in Steubenville, Ohio. Dr. Rahman is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 57 other conditions, according to our data. His clinical expertise encompasses Lung Adenocarcinoma, Small Cell Lung Cancer (SCLC), Paget Disease of the Breast, Bone Marrow Aspiration, and Endoscopy. Dr. Rahman is board certified in American Board Of Internal Medicine and American Board Of Internal Medicine. Dr. Rahman is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Internal Medicine
    Experienced in Dysfibrinogenemia
    Internal Medicine

    Office

    485 Colliers Way Ste E1, 
    Weirton, WV 
     (1.6 miles away)
    Languages Spoken:
    English, Hindi, Punjabi
    Accepting New Patients

    Amar Khurana is a primary care provider, practicing in Internal Medicine in Weirton, West Virginia. Dr. Khurana is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 31 other conditions, according to our data. His clinical expertise encompasses Necrosis, Lung Metastases, Urinary Tract Infection in Children, Gastrostomy, and Endoscopy. Dr. Khurana is currently accepting new patients.

    Experienced in Dysfibrinogenemia
    Cardiology
    Experienced in Dysfibrinogenemia
    Cardiology
    Referral may be required

    Wmc Physician Practices LLC

    651 Colliers Way, Suite 207, 
    Weirton, WV 
     (3.6 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    John Cherian is a Cardiologist practicing medicine in Weirton, West Virginia. Dr. Cherian is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 53 other conditions, according to our data. His clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Hypertension, Necrosis, Pacemaker Implantation, and Endoscopy. Dr. Cherian is currently accepting new patients.

    Learn about our expert tiers
    Experienced in Dysfibrinogenemia
    Family Medicine
    Experienced in Dysfibrinogenemia
    Family Medicine

    Ankle And Foot Care Centers

    332 W 6th St, 
    East Liverpool, OH 
     (14.0 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Theodore Chrobak is a primary care provider, practicing in Family Medicine in East Liverpool, Ohio. Dr. Chrobak is rated as an Experienced provider by MediFind in the treatment of Dysfibrinogenemia. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Bronchitis, Sitosterolemia, Empyema, and Insomnia. Dr. Chrobak is currently accepting new patients.

    Showing 1-4 of 4

    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.