Clinical features
Mutations in LRPAP1 cause an autosomal recessive form of nonsyndromic high myopia, with increased axial length of the globe and decreased visual acuity.
Prevalence
The prevalence of LRPAP1-related conditions cannot be ascertained with precision due to the limited number of cases identified to date.
Inheritance
LRPAP1-related disorder is inherited in an autosomal recessive manner.