Miteva L, Nikolova A
Department of Dermatology and Veneorology, Medical University, Sofia, Bulgaria.
Pediatr Dermatol. 2001 Jan-Feb;18(1):54-6. doi: 10.1046/j.1525-1470.2001.018001054.x.
Various cutaneous and developmental defects of the eyes, teeth, skeleton, and central nervous system have been detected in infants with incontinentia pigmenti. We report an isolated case of incontinentia pigmenti in a 6-month-old girl in association with tricuspid insufficiency, an abnormal shunt of the right pulmonary vein into the superior vena cava, and pulmonary hypertension. We believe that our findings will help to confirm the association of cardiovascular anomalies in IP.
在色素失禁症婴儿中已检测到眼睛、牙齿、骨骼和中枢神经系统的各种皮肤和发育缺陷。我们报告了一例6个月大女童的孤立性色素失禁症病例,该病例伴有三尖瓣关闭不全、右肺静脉异常分流至上腔静脉以及肺动脉高压。我们相信我们的研究结果将有助于证实色素失禁症中心血管异常之间的关联。