Erdem N, Güneş A T, Avci O, Osma E
Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
Dermatology. 1994;188(4):318-21. doi: 10.1159/000247175.
We report a case of Hutchinson-Gilford progeria syndrome (HGPS). The patient showed the characteristics of scleredema at the age of 2.5 months but developed all the manifestations of HGPS gradually until 10 months old. The possibility of development of HGPS should by considered in any case of scleredema at birth or in early infancy.
我们报告一例哈钦森-吉尔福德早衰综合征（HGPS）。该患者在2.5个月大时表现出硬皮病的特征，但直到10个月大时逐渐出现了HGPS的所有表现。对于任何出生时或婴儿早期出现硬皮病的病例，都应考虑HGPS发生的可能性。
