Literature DB >> 2300263

Dopamine-beta-hydroxylase deficiency in humans.

I Biaggioni1, D S Goldstein, T Atkinson, D Robertson.   

Abstract

We report a 42-year-old man with dopamine-beta-hydroxylase deficiency, an autonomic disorder characterized by lifelong severe orthostatic hypotension, ptosis, nasal stuffiness, hyperextensible joints, and retrograde ejaculation. There is isolated deficiency of norepinephrine in both central and peripheral neurons, which contain and release dopamine instead. Dopamine-beta-hydroxylase deficiency should be suspected also in infants presenting with delayed eye opening, hypoglycemia, hypothermia, or hypotension. It can be diagnosed definitively by assay of plasma norepinephrine and dopamine.

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Year:  1990        PMID: 2300263     DOI: 10.1212/wnl.40.2.370

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  17 in total

1.  Neuronal source of plasma dopamine.

Authors:  David S Goldstein; Courtney Holmes
Journal:  Clin Chem       Date:  2008-09-18       Impact factor: 8.327

Review 2.  ATP7A-related copper transport diseases-emerging concepts and future trends.

Authors:  Stephen G Kaler
Journal:  Nat Rev Neurol       Date:  2011-01       Impact factor: 42.937

3.  Catecholamines 101.

Authors:  David S Goldstein
Journal:  Clin Auton Res       Date:  2010-07-11       Impact factor: 4.435

4.  Pediatric ptosis as a sign of treatable autonomic dysfunction.

Authors:  Lara Phillips; David Robertson; Mark R Melson; Emily M Garland; Karen M Joos
Journal:  Am J Ophthalmol       Date:  2013-04-24       Impact factor: 5.258

5.  Predictive value of plasma catecholamine levels in neonatal detection of Menkes disease.

Authors:  S G Kaler; W A Gahl; S A Berry; C S Holmes; D S Goldstein
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

6.  Noninvasive detection of sympathetic neurocirculatory failure.

Authors:  D S Goldstein; C Tack
Journal:  Clin Auton Res       Date:  2000-10       Impact factor: 4.435

7.  Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes.

Authors:  X Fu; P Rinaldo; S H Hahn; H Kodama; S Packman
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

8.  Physical manoeuvres that reduce postural hypotension in autonomic failure.

Authors:  W Wieling; J J van Lieshout; A M van Leeuwen
Journal:  Clin Auton Res       Date:  1993-02       Impact factor: 4.435

9.  Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex.

Authors:  P Cortelli; P Parchi; M Contin; E Sforza; A Lugaresi; R Pasquali; E Lugaresi
Journal:  Clin Auton Res       Date:  1992-06       Impact factor: 4.435

10.  A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia.

Authors:  Anna Bartoletti-Stella; Giacomo Chiaro; Giovanna Calandra-Buonaura; Manuela Contin; Cesa Scaglione; Giorgio Barletta; Annagrazia Cecere; Paolo Garagnani; Paolo Tieri; Alberto Ferrarini; Silvia Piras; Claudio Franceschi; Massimo Delledonne; Pietro Cortelli; Sabina Capellari
Journal:  J Neurol       Date:  2015-09-26       Impact factor: 4.849

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