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Publication year
2007Source
Neuropediatrics, 38, 3, (2007), pp. 148-50ISSN
Publication type
Article / Letter to editor
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Organization
Biochemistry (UMC)
Paediatrics - OUD tm 2017
Journal title
Neuropediatrics
Volume
vol. 38
Issue
iss. 3
Page start
p. 148
Page end
p. 50
Subject
IGMD 3: Genomic disorders and inherited multi-system disorders; IGMD 8: Mitochondrial medicine; NCMLS 2: Metabolism, transport and motion; NCMLS 4: Energy and redox metabolism; ONCOL 3: Translational research; UMCN 5.3: Cellular energy metabolismAbstract
Complex I deficiency is a frequent defect of the mitochondrial electron transport chain. We report on a 3-year-old boy, who rapidly deteriorated after sudden flushing and collapse. This fatal and unusual case was characterized by widely uncontrollable arterial hypertension. It might indicate that hypertensive crisis could be a potential manifestation of mitochondrial disorders.
This item appears in the following Collection(s)
- Academic publications [246764]
- Electronic publications [134220]
- Faculty of Medical Sciences [93461]
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