Factor X deficiency
Factor X deficiency | |
---|---|
Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Easy bruising, nosebleeds, bleeding gums, heavy menstrual periods |
Complications | Hemorrhage |
Onset | Congenital or acquired |
Duration | Lifelong |
Types | N/A |
Causes | Genetic mutation, liver disease, vitamin K deficiency |
Risks | N/A |
Diagnosis | Blood tests, genetic testing |
Differential diagnosis | N/A |
Prevention | N/A |
Treatment | Plasma transfusion, prothrombin complex concentrates |
Medication | N/A |
Prognosis | N/A |
Frequency | Rare |
Deaths | N/A |
Factor X deficiency is a rare bleeding disorder characterized by a deficiency of Factor X, a protein involved in the blood coagulation process. This condition can be either congenital or acquired.
Causes[edit | edit source]
Factor X deficiency can be caused by genetic mutations that affect the production or function of Factor X. It can also be acquired due to conditions such as liver disease, vitamin K deficiency, or the use of certain anticoagulant medications.
Symptoms[edit | edit source]
Individuals with Factor X deficiency may experience symptoms such as:
- Easy bruising
- Nosebleeds
- Bleeding gums
- Heavy menstrual periods
- Prolonged bleeding after injury or surgery
Diagnosis[edit | edit source]
Diagnosis of Factor X deficiency involves blood tests to measure the activity of Factor X. Genetic testing may also be conducted to identify mutations in the F10 gene.
Treatment[edit | edit source]
Treatment options for Factor X deficiency include:
- Plasma transfusion to provide the missing clotting factors
- Administration of prothrombin complex concentrates
- Vitamin K supplementation in cases of deficiency
Complications[edit | edit source]
Without proper management, individuals with Factor X deficiency are at risk of severe hemorrhage, which can be life-threatening.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
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Contributors: Deepika vegiraju, Prab R. Tumpati, MD