Background: Tyrosinase-positive oculocutaneous albinism (OCA, type II, OCA2) is an autosomal recessive genetic disease in which the biosynthesis of melanin decreases in the skin, hair, and eyes. OCA2 disease is caused by mutations in gene. The gene product plays a role in regulating the pH of melanosomes. Up to now, hundreds of mutations have been reported and novel variants are still being discovered.
Methods: In this study, we reviewed the records of OCA2 patients who had conducted albinism genetic testing, and then analyzed the clinical and genetic information of 28 OCA2 patients who had been genetically diagnosed by using Sanger sequencing and next-generation sequencing.
Results: In this study, we reported 31 variants screened from 28 Chinese OCA2 families, and characterized the detailed molecular and clinical presentations. There were 12 novel variants among all detected variants, including 3 missense variants (p.G393V, p.T482A, and p.R720P), 4 frameshift variants (p.R53Gfs49, p.N279Kfs17, p.I469Lfs4, p.I655Nfs12), 2 splicing variants (c.1637-2A > G, c.1951 + 1G > C), 2 stopgain variants (p.L278X, p.W652X) and 1 insertion variants (p.P315LinsT). One potential cluster of missense variants was implicated indicating the important roles of the underlying domains in OCA2 pathogenesis.
Conclusion: Our results were beneficial for diagnosis and precision clinical management for -related disorder, and this study expanded the mutation spectrum of oculocutaneous albinism.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8544823 | PMC |
| http://dx.doi.org/10.3389/fgene.2021.715437 | DOI Listing |
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Article Synopsis
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