𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17

✍ Scribed by Astrid Rasmussen; Irene De Biase; Marcela Fragoso-Benítez; Marco Antonio Macías-Flores; Petra Yescas; Adriana Ochoa; Tetsuo Ashizawa; María Elisa Alonso; Sanjay I. Bidichandani


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
156 KB
Volume
61
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Spinocerebellar ataxia type 17 (SCA17) is caused by expansion of a CAG/CAA repeat in the TBP gene. Most pathogenic alleles are interrupted and are stably transmitted from parent to offspring without anticipation. We identified three SCA17 families with expansion of uninterrupted alleles, thus greatly increasing the number of known intergenerational transmissions of such alleles. We found that uninterrupted SCA17 alleles are unstable, associated with anticipation, and show a paternal expansion bias that increases with age. Even small increments in repeat length resulted in inordinate increases in anticipation. Anticipation was also associated with childhood presentation. Sequencing of all SCA17 alleles is required for effective genetic counseling. Ann Neurol 2007


📜 SIMILAR VOLUMES


Spinocerebellar ataxia type 2 (SCA 2) in
✍ Babovic-Vuksanovic, Dusica; Snow, Karen; Patterson, Marc C.; Michels, Virginia V 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 16 KB 👁 2 views

Autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. Spinocerebellar ataxia type 2 typically presents with progressive cerebellar symptoms, slow ocular saccades, and peripheral neuropathy. The onset of symptoms is usually

Somatic mosaicism of the CAG repeat expa
✍ Géraldine Cancel; Isabelle Gourfinkel-An; Giovanni Stevanin; Olivier Didierjean; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB

An expanded and unstable CAG repeat in the coding region of the MJD1 gene is the mutation responsible for spinocerebellar ataxia 3/Machado-Joseph disease. In order to determine whether there was a higher degree of instability in affected regions, the size of the expanded CAG repeat was analyzed in d