A hitherto unreported bilateral and symmetrical hypopigmentary anomaly is reported in five members of a Negro family. The pattern of inheritance would appear to be autosomal dominant and it is concluded that this is a benign pigmentary alteration unrelated to underlying disease.
WEARY PE, BEHLEN CH. Unusual Familial Hypopigmentary Anomaly. Arch Dermatol. 1965;92(1):54–55. doi:10.1001/archderm.1965.01600130060009
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