Genetic testing and prenatal diagnosis for thirteen Chinese pedigrees affected with oculocutaneous albinism.
10.3760/cma.j.cn511374-20210201-00100
- Author:
Yujiao YANG
1
;
Bin MAO
;
Qiong WANG
;
Shubing LIE
;
Ruixuan ZHANG
;
Xiuli ZHAO
Author Information
1. Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences - School of Basic Medicine, Peking Union Medical College, Beijing 100005, China. xiulizhao@ibms.pumc.edu.cn.
- Publication Type:Journal Article
- MeSH:
Albinism, Oculocutaneous/genetics*;
China;
Female;
Genetic Testing;
Humans;
Membrane Transport Proteins/genetics*;
Monophenol Monooxygenase/genetics*;
Mutation;
Pedigree;
Pregnancy;
Prenatal Diagnosis
- From:
Chinese Journal of Medical Genetics
2022;39(2):143-147
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To identify the causative variants in 13 Chinese pedigrees affected with oculocutaneous albinism (OCA) so as to provide genetic counseling and prenatal diagnosis to them.
METHODS:Thirteen unrelated pedigrees with clinically diagnosed OCA were collected and classified based on the manifestation of skin and eyes. With informed consent obtained from the participants, peripheral blood samples were collected from the probands and their family members for the extraction of genomic DNA. Candidate variants were screened by targeted capture and next generation sequencing, and the results were validated by Sanger sequencing. Prenatal diagnosis was provided to the families upon their subsequent pregnancies.
RESULTS:Causative variants were detected in all probands, including 10 with compound heterozygotes or homozygotes for TYR gene variants and 3 with compound heterozygotes for OCA2 gene variants. Among these, two variants [TYR: c.650G>C (p.Arg217Pro) and OCA2: c.516-2A>T] were unreported previously. The pathogenicity of the novel TYR: c.650G>C (p.Arg217Pro) variant was verified through bioinformatic analysis and prediction of three dimensional structure of the protein. Prenatal diagnosis was provided to 6 fetuses with a high risk for OCA. Four fetuses were found to be carriers, one did not carry the variants of the proband, and one was affected with OCA.
CONCLUSION:Identification of the pathogenic variants in the 13 probands, including 2 novel ones, has expanded the mutational spectrum of OCA and enabled genetic counseling and prenatal diagnosis for the families.
