https://pmc.ncbi.nlm.nih.gov/articles/PMC4745298/
Osteoporosis-Pseudoglioma in a Mauritanian Child due to a Novel Mutation in LRP5 - PMC
Osteoporosis-pseudoglioma (OPPG) syndrome is a very rare autosomal recessive disorder, caused by mutations in the low-density lipoprotein receptor-related...
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