Mitochondrial encephalomyopathies starting in childhood and adolescence

M. Castro-Gago, M.I. Novo-Rodríguez, J. Eirís-Puñal Revisión ● Views 1123 ● Downloads 251 Castellano English

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DOI: https://doi.org/10.33588/rn.26S1.98038

INTRODUCTION. In this chapter we carry out a review of the current basic clinical and diagnostic aspects of mitochondrial cytopathies due to deficiencies in the mitochondrial respiratory chain complexes, which appear clinically during childhood and/or adolescence. DEVELOPMENT. The description has been divided into two groups: mitochondrial cytopathies secondary to alterations of the mitochondrial DNA (mtDNA) and mitochondrial cytopathies secondary to alterations of the nuclear DNA (nDNA).

CONCLUSIONS. We conclude by considering the importance of such conditions at this age

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Mitochondrial encephalomyopathies starting in childhood and adolescence

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