Hereditary factor XIII deficiency (Q63970): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 11:28, 14 August 2026
Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2079957863 |
||
| English | Hereditary factor XIII deficiency |
Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected. |
Statements
CID11:ID_2079957863
0 references
dki-india-ID_2079957863
0 references
Concluído
0 references
