| Autor: |
Janson, Christopher G., Kolodny, Edwin H., Zeng, Bai‐Jin, Raghavan, Srinivasa, Pastores, Gregory, Torres, Paola, Assadi, Mitra, McPhee, Scott, Goldfarb, Olga, Saslow, Beth, Freese, Andrew, Wang, D. J., Bilaniuk, Larissa, Shera, David, Leone, Paola |
| Zdroj: |
Annals of Neurology; February 2006, Vol. 59 Issue: 2 p428-431, 4p |
| Abstrakt: |
We describe two sisters with a mild‐onset variant of Canavan's disease who presented at age 50 and 19 months with developmental delay but without macrocephaly, hypotonia, spasticity, or seizures. Remarkably, both patients had age‐appropriate head control, gross motor development, and muscle tone. There were very mild deficits in fine motor skills, coordination, and gait. Both sisters had a history of strabismus, but otherwise vision was normal. The older child showed evidence of mild cognitive and social impairment, whereas language and behavior were normal for age in the infant. Both patients were found to be compound heterozygotes for C914A (A305E) and G212A (R71H) mutations in ASPA. Like all other known ASPAmutations, this previously unknown G212A mutation appears to have low absolute enzyme activity. Nevertheless, it is associated in these patients with an extremely benign phenotype that is highly atypical of Canavan's disease. Biochemical and clinical data were evaluated using a generalized linear mixed model generated from 25 other subjects with Canavan's disease. There were statistically significant differences in brain chemistry and clinical evaluations, supporting a distinct variant of Canavan's disease. Future studies of ASPA enzyme structure and gene regulation in these subjects could lead to a better understanding of Canavan's pathophysiology and improvements in ASPAgene therapy Ann Neurol 2006;59:428–431 |
| Databáze: |
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