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Ann Neurol ; 61(6): 607-10, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17474109

RESUMEN

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.


Asunto(s)
Anticipación Genética , Ataxias Espinocerebelosas/genética , Proteína de Unión a TATA-Box/genética , Expansión de Repetición de Trinucleótido/genética , Adolescente , Adulto , Edad de Inicio , Alelos , Niño , Progresión de la Enfermedad , Femenino , Humanos , Masculino , México , Persona de Mediana Edad , Linaje , Distribución por Sexo , Ataxias Espinocerebelosas/diagnóstico
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