ADP platelet receptor P2Y12 deficiency (Q84808): Difference between revisions
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A deficiência congênita do receptor plaquetário do ADP (P2Y12) é um raro transtorno autossômico recessivo de plaquetas que dá origem a uma síndrome de sangramento leve marcada por perda sanguínea excessiva pós traumática e pós cirúrgica. | |||
| description / en | description / en | ||
Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss. | |||
Revision as of 10:09, 15 August 2026
Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_121084770 |
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| English | ADP platelet receptor P2Y12 deficiency |
Congenital deficiency of the P2Y12 ADP receptor is a rare autosomal recessive disorder of platelets that gives rise to a mild bleeding syndrome marked by excessive posttraumatic and postsurgical blood loss. |
