Bleeding diathesis due to integrin alpha2-beta1 deficiency (Q100852): Difference between revisions

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Susceptibilidade incomum a sangramento (hemorragia) majoritariamente devida a hipocoagulabilidade, por sua vez causada por uma coagulopatia (um defeito no sistema da coagulação). Este diagnóstico é devido a uma deficiência nos receptores transmembrana que mediam a ligação entre a célula e os tecidos que a cercam, como as outras células e a matriz extracelular (MEC).
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This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).

Revision as of 17:37, 16 August 2026

This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).
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ID_1508140529
    English
    Bleeding diathesis due to integrin alpha2-beta1 deficiency
    This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).

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