Psychiatric disturbances in five patients with MELAS syndrome
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Kierownik: prof. dr n. med. J. Zeman, Katedra Medycyny Dzieci i Młodzieży, Pierwszy Wydział Medycyny Uniwersytetu Karola w Pradze
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Kierownik: prof. dr n. med. J. Raboch, Katedra Psychiatrii, Pierwszy Wydział Medycyny Uniwersytetu Karola w Pradze
Submission date: 2014-01-13
Final revision date: 2014-03-06
Acceptance date: 2014-03-08
Publication date: 2014-10-31
Corresponding author
Jiri Zeman
Kierownik: prof. dr n. med. J. Zeman, Katedra Medycyny Dzieci i Młodzieży, Pierwszy Wydział Medycyny Uniwersytetu Karola w Pradze, Ke Karlovu 2, 120 00 Prague 2, Czech Republic
Psychiatr Pol 2014;48(5):1035-1045
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ABSTRACT
Objectives:
Mitochondrial disorders of energetic metabolism (MD) represent a heterogeneous group of diseases manifesting at any age with a broad spectrum of clinical symptoms, including psychiatric disorders.
Methods:
The aim of the study was to characterize psychiatric symptoms and diagnoses in five patients with MELAS syndrome between the ages of 17 and 53 year.
Results:
Four of MELAS patients them harbored the prevalent mitochondrial DNA (mtDNA) mutation 3243A>G, and one patient had the mtDNA mutation 12706T>C. Three patients had positive family histories for MELAS syndrome. In one patient, depression was diagnosed as the first symptom of MELAS syndrome. Depression also preceded a stroke-like episode in one patient. Four patients had disturbed cognitive functions, confusional states occurred in three patients. One patient manifested psychotic (schizophrenia-like) symptom.
Conclusions:
Mitochondrial disorders deserve consideration as part of the differential diagnosis, especially if there is suspected involvement of other organ groups or positive family history of MD.