Carrier detection of Batten disease (Juvenile neuronal ceroid-lipofuscinosis)

✍ Scribed by Taschner, Peter E. M. ;de Vos, Nanneke ;Post, Jan G. ;Meijers-Heijboer, E. Johanna ;Hofman, Irene ;Loonen, M. Christa B. ;Pinckers, Alfred J. L. G. ;Bleeker-Wagemakers, Elisabeth M. ;Gardiner, R. Mark ;Breuning, Martijn H.

• Publisher: John Wiley and Sons
• Year: 1995
• Tongue: English
• Weight: 467 KB
• Volume: 57
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.1320570246

✦ Synopsis

Batten disease, or the juvenile form of neuronal ceroid lipofuscinosis, is an autosomal recessive neurodegenerative disorder manifesting with progressive blindness, seizures, and dementia, leading to an early death. The CLN3 locus which is involved in Batten disease had been localized to chromosome 16~11.2. Linkage disequilibrium has been observed between CLN3 and polymorphic microsatellite markers D16S288, D16S299, and D16S298, making carrier detection and prenatal diagnosis by haplotype analysis possible. For the purpose of carrier detection, haplotypes from Dutch Batten patients and their families were constructed. Most patients share the same D16S298 allele, suggesting the presence of a founder effect in the Dutch population. In a large inbred Dutch family, in which Batten disease occurs with high frequency, haplotype analysis has been carried out with high accuracy for carrier detection.