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General Information:
Id:
7,552
Diseases:
Neurological
Homo sapiens
article/cited
Reference:
Arnold AC et al.(2017) Hyperinsulinemia and Insulin Resistance in Dopamine beta-Hydroxylase Deficiency J. Clin. Endocrinol. Metab. 102: 10-14
[PMID: 27778639]
Interaction Information:
Comment
Dopamine beta-hydroxylase deficiency is a rare genetic disorder characterized by failure to convert dopamine to norepinephrine. (cited information)
Dopamine beta-hydroxylase deficiency is a rare genetic disorder characterized by failure to convert dopamine to norepinephrine (Noradrenaline). Due to the defect in the enzyme dopamine beta-hydroxylase levels of plasma norepinephrine and epinephrine are undetectable and dopamine levels are high. (cited information)
Dopamine beta-hydroxylase deficiency is a rare genetic disorder characterized by failure to convert dopamine to norepinephrine (Noradrenaline). Due to the defect in the enzyme dopamine beta-hydroxylase levels of plasma norepinephrine and epinephrine are undetectable and dopamine levels are high. (cited information)
Dopamine beta-hydroxylase deficiency is a rare genetic disorder characterized by failure to convert dopamine to norepinephrine (Noradrenaline). (cited information)