Caksen H, Cesur Y, Odabas D, Aslan H, Rastgeldi L
Department of Pediatrics, YüzüncüYil University of Medicine, Van, Turkiye.
J Nippon Med Sch. 2001 Oct;68(5):442-3. doi: 10.1272/jnms.68.442.
Infantile cortical hyperosteosis (ICH) is usually a self-limited disease of infancy with bony changes, soft tissue swelling, fever, irritability, decreased appetite, and decreased movement of the affected bones. Its description in isolated patients or in multiple members of families suggests the existence of two different forms, namely a sporadic form and a familial form with incomplete penetrance. In this article, we report a 2.5-month-old girl with ICH of sporadic form, due to unusual presentation.
婴儿皮质增生症(ICH)通常是一种婴儿期的自限性疾病,伴有骨质改变、软组织肿胀、发热、易激惹、食欲减退以及患骨活动减少。对个别患者或家族中多名成员的描述表明存在两种不同形式,即散发型和外显不全的家族型。在本文中,我们报告了一名2.5个月大患散发型ICH的女童,因其表现不寻常。