Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 19, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Differential Diagnosis for Thrombophilia Condition

Given the patient's laboratory results, the following differential diagnoses are considered:

  • Single Most Likely Diagnosis

    • Antiphospholipid Syndrome (APS): This condition is characterized by the presence of lupus anticoagulant, which is positive in this patient, and is known to cause thrombosis. The low Protein S activity also supports this diagnosis, as APS can lead to acquired Protein S deficiency.
  • Other Likely Diagnoses

    • Acquired Protein S Deficiency: Although the patient's Protein C and antithrombin III levels are normal, the isolated low Protein S activity could indicate an acquired deficiency, which can be due to various factors including APS, nephrotic syndrome, or vitamin K deficiency.
    • Other Acquired Thrombophilias: Conditions such as cancer, autoimmune disorders, or chronic infections can lead to acquired thrombophilia, which might not be directly indicated by the provided lab results but should be considered given the clinical context.
  • Do Not Miss Diagnoses

    • Disseminated Intravascular Coagulation (DIC): Although less likely given the normal antithrombin III and Protein C levels, DIC can present with a variety of coagulation abnormalities, including low Protein S. It's a critical condition that requires prompt recognition and treatment.
    • Severe Vitamin K Deficiency: This could potentially lead to low Protein S activity (as well as other vitamin K-dependent clotting factors), although the normal Protein C level makes this less likely.
  • Rare Diagnoses

    • Protein S Deficiency Due to a Rare Genetic Mutation: While the patient's family history and other genetic tests are not provided, a rare genetic mutation affecting Protein S could be considered, especially if other explanations are ruled out.
    • Other Rare Thrombophilic Conditions: Conditions such as heparin cofactor II deficiency, or specific genetic mutations affecting other parts of the coagulation pathway, are rare but could potentially explain the patient's presentation if more common causes are excluded.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.