Teebi A S, Shaabani I S
Department of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510.
Am J Med Genet. 1993 Aug 15;47(2):166-8. doi: 10.1002/ajmg.1320470204.
We report on a 6-year-old girl with Costello syndrome. Main manifestations included poor postnatal growth, relative macrocephaly, curly hair, distinct "coarse" face, mild mental retardation, happy and sociable personality, loose dark skin particularly of hands and feet, acanthosis nigricans, thin deep set nails, enamel hypoplasia of teeth, and hyperextensible joints. The absence to date of perioral and nasal papillomata in this girl suggests that Costello syndrome is clinically recognizable even before appearance of such papillomata. Manifestations are compared to the four previously reported sporadic cases.
我们报告了一名患有科斯特洛综合征的6岁女孩。主要表现包括出生后生长发育迟缓、相对巨头畸形、卷发、独特的“粗糙”面容、轻度智力障碍、性格开朗且善于社交、手部和足部等部位皮肤松弛黝黑、黑棘皮病、指甲薄且深陷、牙齿釉质发育不全以及关节过度伸展。该女孩目前尚无口周和鼻周乳头状瘤,这表明科斯特洛综合征在这些乳头状瘤出现之前在临床上也是可识别的。将这些表现与之前报道的4例散发病例进行了比较。