| Literature DB >> 17092469 |
Denise Cassandrini1, Salvatore Savasta, Mauro Bozzola, Alessandra Tessa, Marina Pedemonte, Stefania Assereto, Silvia Stringara, Carlo Minetti, Filippo M Santorelli, Claudio Bruno.
Abstract
We report an 11-year-old boy with short stature, bilateral ptosis, sensorineural hearing loss, muscle weakness, and endocrine abnormalities. Brain magnetic resonance imaging (MRI) showed a bilateral abnormal signal in the globus pallidus and in the midbrain tegment. Muscle biopsy specimens showed ragged red and cytochrome c oxidase negative fibers, and biochemical analysis of muscle homogenate showed a partial defect of complex I and IV activities of the respiratory chain enzymes. Analysis of mitochondrial DNA by a polymerase chain reaction screening procedure and Southern blot revealed a novel heteroplasmic single mitochondrial DNA deletion of 7.8 kb in different tissues. This deletion was absent in the blood DNA of his mother and brother. This case further expands and confirms the wide clinical spectrum of mitochondrial disorders associated with single large-scale mitochondrial DNA deletions.Entities:
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Year: 2006 PMID: 17092469 DOI: 10.1177/08830738060210111001
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987