Norepinephrine transporter deficiency (Q83854): Difference between revisions
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Condição caracterizada por taquicardia ortostática excessiva, hipertensão, síncope e está associada a depuração de norepinefrina e de epinefrina prejudicada, hipersensibilidade de receptores adrenérgicos e uma resposta pressórica diminuída à tiramina. Em uma família, esta síndrome foi causada por uma mutação na proteína transportadora de norepinefrina. | |||
| description / en | description / en | ||
This is a condition characterised by excessive orthostatic tachycardia, hypertension, syncope and is associated with impaired norepinephrine and epinephrine clearance, hypersensitivity of adrenergic receptors and a decreased pressor response to tyramine. In one family this syndrome was caused by a mutation in the norepinephrine transporter protein. | |||
Revision as of 09:13, 15 August 2026
This is a condition characterised by excessive orthostatic tachycardia, hypertension, syncope and is associated with impaired norepinephrine and epinephrine clearance, hypersensitivity of adrenergic receptors and a decreased pressor response to tyramine. In one family this syndrome was caused by a mutation in the norepinephrine transporter protein.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_296781205 |
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| English | Norepinephrine transporter deficiency |
This is a condition characterised by excessive orthostatic tachycardia, hypertension, syncope and is associated with impaired norepinephrine and epinephrine clearance, hypersensitivity of adrenergic receptors and a decreased pressor response to tyramine. In one family this syndrome was caused by a mutation in the norepinephrine transporter protein. |
