Hereditary vitamin K-dependent coagulation factors deficiency (Q67792): Difference between revisions
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Doença causada por mutações geneticamente herdadas. Essa doença é caracterizada por níveis baixos de vitamina K no organismo, levando a anormalidades na coagulação sanguínea. Pode apresentar-se com sangramento prolongado e hemorragias. A confirmação é feita pela identificação de mutações por testagem genética. | |||
| description / en | description / en | ||
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing. | |||
Revision as of 15:37, 14 August 2026
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1818851075 |
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| English | Hereditary vitamin K-dependent coagulation factors deficiency |
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing. |
