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Mitochondrial Dysfunction in Patients With Hypotonia, Epilepsy, Autism, and Developmental Delay: HEADD Syndrome

Departments of Pediatrics, Dartmouth Hitchcock Medical Center, Lebanon, NH.

Michael J. Goldenthal, PhD

Molecular Cardiology and Neuromuscular Institute, Highland Park, NJ, Dartmouth Hitchcock Medical Center, Lebanon, NH.

C. Harker Rhodes, MD, PhD

Departments of Pathology, Dartmouth Hitchcock Medical Center, Lebanon, NH.

José Marin-Garcia, MD

Molecular Cardiology and Neuromuscular Institute, Highland Park, NJ, Dartmouth Hitchcock Medical Center, Lebanon, NH, tmci{at}att.net

A group of 12 children clinically presenting with hypotonia, intractable epilepsy, autism, and developmental delay, who did not fall into previously described categories of mitochondrial encephalomyopathy, were evaluated for mitochondrial respiratory enzyme activity levels, mitochondrial DNA, and mitochondrial structural abnormalities. Reduced levels in specific respiratory activities were found solely in enzymes with subunits encoded by mitochondrial DNA in seven of eight biopsied skeletal muscle specimens evaluated. Five cases exhibited increased levels of large-scale mitochondrial DNA deletions, whereas pathogenic point mutations previously described in association with mitochondrial encephalomyopathies were not found. Mitochondrial structural abnormalities were present in three of four patients examined. Our findings suggest that mitochondrial dysfunction, including extensive abnormalities in specific enzyme activities, mitochondrial structure, and mitochondrial DNA integrity, may be present in children with a clinical constellation including hypotonia, epileptic seizures, autism, and developmental delay. The acronym HEADD is presented here to facilitate pursuit of mitochondrial defects in patients with this clinical constellation after other causes have been excluded. (J Child Neurol 2002;17:435-439).

Journal of Child Neurology, Vol. 17, No. 6, 435-439 (2002)
DOI: 10.1177/088307380201700607


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