Вроджений дефіцит фактора XIII
ORPHA:331· ICD-10 D68.2· Congenital factor XIII deficiency
Визначення(English summary)
Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal recessive, Not applicable
- Вік початку
- All ages