Kojmane W, Hmami F, Atmani S
Service de néonatologie et réanimation néonatale, CHU Hassan II, Fès, Maroc.
Service de néonatologie et réanimation néonatale, CHU Hassan II, Fès, Maroc.
Ann Dermatol Venereol. 2019 Mar;146(3):223-225. doi: 10.1016/j.annder.2018.11.009. Epub 2019 Jan 9.
Adams-Oliver syndrome (AOS) is a congenital condition characterized by congenital aplasia cutis and transverse limb defects. Herein we report a case of an infant with severe intra-uterine growth restriction presenting AOS associated with cutis marmorata telangiectatica but with no other organ complications. The outcome was complicated by hemorrhagic and septic shock, which resulted in the death of the infant in a setting of multiorgan failure.
亚当斯-奥利弗综合征(AOS)是一种先天性疾病,其特征为先天性皮肤发育不全和肢体横断性缺损。在此,我们报告一例患有严重宫内生长受限的婴儿,该婴儿表现为AOS并伴有先天性网状青斑,但无其他器官并发症。结局因出血性和感染性休克而复杂化,这导致婴儿在多器官功能衰竭的情况下死亡。