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At 26, the individual had prophylactic laser treatment for lattice deterioration for the retina. At 32, she was discovered becoming heterozygous for the c.1527 GT variant in the COL2A1 gene, which is associated with ocular abnormalities and autosomal dominant form of Stickler problem. Later, she wished to go after prenatal diagnostic evaluating when it comes to familial variation. The patient voiced that the results would influence maternity management. Amniocentesis was carri
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