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. 2022 Jan 19;43(3):380–388. doi: 10.1002/humu.24327

Figure 2.

Figure 2

Pedigree of family II, index patient A has confirmed mutations in the ARR3 gene. Aunts D and C have high myopia. Nieces G and L have high myopia; moreover, niece G suffered Retinal detachment at age 18. Deceased grandma M and her deceased mother O and her deceased sister N all were affected by high myopia. The familial pathogenic variant was segregated in aunt D and niece G