Adamicová Katarína, Balhárek Tomáš, Lúčanová Lucia, Nyitrayová Oľga, Fetisovová Zelmíra
Cesk Patol. 2014;50(4):155-8.
Barts syndrome, in literature also known under the name CLAS (Congenital Localised Absence of Skin), first described by Bart in 1966 as congenital localized absence of skin, epidermolysis bullosa congenita and nail abnormalities. The authors present a macroscopic and histological findings of a newborn with Barts syndrome, with epidermolysis bullosa junctionalis and atresia pylori, who died 17 days after birth and 13 days after surgery for pyloric stenosis.
巴茨综合征,在文献中也被称为CLAS(先天性局限性皮肤缺失),1966年由巴特首次描述为先天性局限性皮肤缺失、先天性大疱性表皮松解症和指甲异常。作者展示了一名患有巴茨综合征、交界性大疱性表皮松解症和先天性幽门闭锁的新生儿的大体和组织学检查结果,该新生儿出生后17天、幽门狭窄手术后13天死亡。