Suskind R, Esterly N B
Birth Defects Orig Artic Ser. 1971 Jun;7(8):103-6.
Congenital hypertrichosis universalis is a rare familial disorder felt to be inherited as an autosomal dominant trait. The patient described below was noted to have excessive body hair at birth. The hairiness increased progressively. By two years of age, the patient's face, trunk and limbs were covered with long hair. Only the mucous membranes, palms and soles were spared. The patient's father and paternal grandfather were also noted to be hirsute at birth.
全身性先天性多毛症是一种罕见的家族性疾病，被认为是作为常染色体显性性状遗传的。以下描述的患者在出生时就被注意到有过多的体毛。毛发逐渐增多。到两岁时，患者的面部、躯干和四肢都覆盖着长毛。只有黏膜、手掌和脚底没有毛发。还注意到患者的父亲和祖父在出生时也多毛。
