Factor X deficiency: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 56: Line 56:
[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Rare diseases]]
[[Category:Rare diseases]]
<gallery>
File:Autosomal recessive - en.svg|Factor X deficiency
</gallery>

Latest revision as of 00:41, 20 February 2025


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]

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]

Individuals with Factor X deficiency may experience symptoms such as:

Diagnosis[edit]

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]

Treatment options for Factor X deficiency include:

Complications[edit]

Without proper management, individuals with Factor X deficiency are at risk of severe hemorrhage, which can be life-threatening.

See also[edit]

References[edit]

<references group="" responsive="1"></references>


External links[edit]