Hypergonadotropic Hypogonadism in Spinocerebellar Ataxia Type 2: A Case Report

The present study suggests that a common genetic implication may be shared between these neurologic and non-neurologic signs, and there may be various associations between these heterogeneous manifestations. The clinical spectrum of the SCA2 should be widened, and further data collection is needed to elucidate the relationship among the clinical manifestations. Kwon D-Y, and Park MH. Hypergonadotropic hypogonadism in spinocerebellar ataxia type 2: A case report.