Hypoplasminogenaemia (Q43087): Difference between revisions
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Hipoplasminogenemia grave ou deficiência de plasminogênio (plg) tipo I é uma doença sistêmica caracterizada por fibrinólise extracelular acentuadamente comprometida, levando à formação de pseudomembranas lenhosas (ricas em fibrina) em mucosas durante a cicatrização de feridas. | |||
| description / en | description / en | ||
Severe hypoplasminogenaemia or type 1 plasminogen (plg) deficiency is a systemic disease characterised by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae during wound healing. | |||
Revision as of 09:54, 13 August 2026
Severe hypoplasminogenaemia or type 1 plasminogen (plg) deficiency is a systemic disease characterised by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae during wound healing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | DA0D.3 |
||
| English | Hypoplasminogenaemia |
Severe hypoplasminogenaemia or type 1 plasminogen (plg) deficiency is a systemic disease characterised by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae during wound healing. |
