Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy?
The Authors report on a patient with Kearns-Sayre syndrome, large mtDNA deletion (7/kb), facial abnormalities and severe central nervous system (CNS) white matter radiological features, commonly attributed to spongy alterations. The common origin from neural crest cell (NCC) of facial structures (ca...
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Main Authors: | Agostino Berio (Author), Attilia Piazzi (Author), Carlo Enrico Traverso (Author) |
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Format: | Book |
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PAGEPress Publications,
2017-12-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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