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PubMed · 9445918

[Mitochondrial diseases].

J D Nagel·F Haverkamp·M J Lentze
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Abstract

Mitochondrial disease are a heterogeneous group, combining multiple symptoms resulting from defects in various organs. Thus identification of a particular mitochondrial disease due to clinical symptoms is not possible. However, simple biochemical tests can provide guiding and reliable results quickly. We present a classification of the mitochondrial diseases, describing important clinical symptoms and explaining a diagnostic plan to identify defects of biochemical mitochondrial pathways.

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Abnormalities, MultipleAcetyl Coenzyme AAdolescentChildChild, PreschoolChromosome AberrationsChromosome DisordersDNA, MitochondrialDiagnosis, DifferentialFemaleHumansInfantInfant, NewbornMaleMitochondrial EncephalomyopathiesMitochondrial MyopathiesPyruvic AcidEnglish AbstractJournal ArticleReview

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J D Nagel, F Haverkamp, M J Lentze. [Mitochondrial diseases].. https://doi.org/10.1055/s-2008-1043974

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