Bull M J, Norins A L, Weaver D D, Weber T, Mitchell M
Am J Dis Child. 1983 May;137(5):449-51.
A sister and brother each had epidermolysis bullosa and pyloric atresia at birth. Both died in early infancy of complications related to epidermolysis bullosa. Electron microscopic studies of skin biopsy specimens disclosed findings consistent with a diagnosis of epidermolysis bullosa letalis. The existence of epidermolysis bullosa-pyloric atresia syndrome as a distinct clinical entity with autosomal recessive inheritance is supported by the findings in these patients.
一名姐弟出生时均患有大疱性表皮松解症和幽门闭锁。两人均在婴儿早期死于与大疱性表皮松解症相关的并发症。皮肤活检标本的电子显微镜研究结果与致死性大疱性表皮松解症的诊断相符。这些患者的研究结果支持了大疱性表皮松解症 - 幽门闭锁综合征作为一种具有常染色体隐性遗传的独特临床实体的存在。