Vitamin K Deficiency - Hemorrhagic Disease of the Newborn (HDN)

Vitamin K Deficiency | Hemorrhagic Disease of the Newborn or Vitamin K dependent bleeding (VKDB) is a bleeding disorder that occurs due to deficiency of vitamin K.

Factor XIII Deficiency | Fibrin Stabilizing Factor Defect.

Factor X Deficiency is an autosomal recessive disease. In factor X deficiency, there is a coagulation (secondary Hemostasis) defect.

In a previous video: we discussed "hemophilia A, Hemophilia B, and Hemophilia C | A Comparison."

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Hemophilia is a genetic Coagulation Disorder characterized by abnormally excessive bleeding 🩸 even after a minor scratch. Hemophilia is divided into three subtypes: hemophilia A, hemophilia B, and hemophilia C. Hemophilia A and hemophilia B are X-linked recessive, whereas hemophilia C is autosomal recessive.'

Coagulation Tests (PT, aPTT, TT, Fibrinogen, Mixing Studies,..etc).
The coagulation factors are divided into 3 coagulation groups | Fibrinogen group, Prothrombin group, and Contact Group..

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Platelet count is one of the lab tests used by a doctor or a hematologist to assess whether your platelet number is normal, low (thrombocytopenia) or high (thrombocytosis).

Bleeding 🩸 time (BT) is another test for platelet function.

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