Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis.
Clara VidicMarcin ZaniewSzymon JurgaHolger ThieleHeiko ReutterAlina C HilgerPublished in: Molecular and cellular pediatrics (2021)
To the best of our knowledge, this is the first report of early onset dysfunctional voiding, seizures, and bilateral spasticity of the lower limbs associated with a novel heterozygous dominant missense variant in DSTYK.