LRPAP1

Professionals

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.