van Benthem L H, Bijlsma J B, Delemarre-van de Waal H A
Tijdschr Kindergeneeskd. 1981 Jun;49(3):86-92.
A tall 15 1/2-year-old-girl with an xxx sex chromosome complement, absence of secondary sexual characteristics and histologically verified pure gonadal dysgenesis is described. In contrast to patients with an xxy sex chromosome configuration who--after puberty--are recognisable by typical somatic abnormalities, triple-x females generally show no physical anomalies. Speech and language problems can be features of the triple-x condition; ovarian dysfunction in triple-x females has been described only sporadically. Probably one patient is the second case described having this chromosomal aberration combined with pure gonadal dysgenesis. The presence of three x chromosomes (and thereby possibly extra growth determinants) could be the reason for the extra growth potential in these patients. This contrasts with the reduced growth in patients with the xo sex chromosome configuration who tend to remain small.
描述了一名15岁半的高个子女孩,其性染色体组成为xxx,缺乏第二性征,且经组织学证实为单纯性腺发育不全。与青春期后可通过典型躯体异常识别的xxy性染色体构型患者不同,三体X女性通常没有身体异常。言语和语言问题可能是三体X综合征的特征;三体X女性的卵巢功能障碍仅偶尔有描述。可能有一名患者是第二例被描述为具有这种染色体畸变并伴有单纯性腺发育不全的病例。三条X染色体的存在(从而可能有额外的生长决定因素)可能是这些患者具有额外生长潜力的原因。这与XO性染色体构型患者生长受限形成对比,后者往往身材矮小。