| Autor: |
Komaki, H., Sasaki, M., Ishiyama, A., Nishino, I., Makioka, N., Ogata, T., Suzuki, E., Muramatsu, K., Sakai, C., Matsushima, Y., Goto, Y.‐I., Uchino, S., Mimaki, M. |
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| Zdroj: |
Clinical Genetics; May2018, Vol. 93 Issue 5, p1103-1106, 5p, 1 Black and White Photograph, 1 Diagram, 1 Chart |
| Abstrakt: |
Genetic abnormalities in mitochondrial complex assembling factors are associated with leukoencephalopathy. We present a 1‐year‐old girl with consciousness disturbance after a respiratory infection. Brain MRI revealed leukoencephalopathy with bilaterally symmetrical hyperintensity in the substantia nigra, medial thalamic nuclei, and basal nuclei, as well as cavities in the cerebral white matter and corpus callosum. Lactate levels in the spinal fluid were high, while magnetic resonance spectroscopy of the cerebral white matter and basal nuclei showed high peak lactate levels, suggesting mitochondrial dysfunction. The respiratory enzyme activity of complex I was reduced to 17% to 21% in skeletal muscle. Whole exome sequencing identified compound heterozygous variations in NDUFAF3, involved in the assembly of mitochondrial complex I (c.342_343insGTG:p.117Valdup, c.505C > A:p.Pro169Thr). Two‐dimensional, blue‐native polyacrylamide gel electrophoresis (PAGE) and sodium dodecyl sulfate‐PAGE revealed reductions in Q‐module (NDUFS2, NDUFS3, and NDUFA9) and P‐module (NDUFB10 and NDUFB11) subunits, indicating disruption of mitochondrial complex I assembly. Our report expands the spectrum of clinical phenotypes associated with pathogenic variants of NDUFAF3. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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