Norepinephrine transporter deficiency (Q83854): Difference between revisions
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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 |
||
| 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. |
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CID11:ID_296781205
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dki-india-ID_296781205
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