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. 2021 Dec 8;12:773922. doi: 10.3389/fgene.2021.773922

TABLE 1.

Characteristic features of WS3 in Family D.

Status Member Deafness Heterochromic iridis Premature graying of the hair Dystopia canthorum Patchy de-pigmentation of the skin Limb anomaly
Affected II-1 Left ear N N Y N N
Affected II-2 Right ear Both Y Y N N
Unaffected II-3 N N N N N N
Unaffected II-4 N N N N N N
Affected II-5 N N N Y N N
Affected III-1 Left ear Right eye Y Y N N
Unaffected III-2 N N N N N N
Affected III-3 Both Right eye N Y N N
Unaffected III-4 N N N N N N
Unaffected III-5 N N N N N N
Affected III-6 Both Both N Y Y Y