新生儿天生性胃壁肌层缺损并穿孔是一种较少见的消化道疾病。我院于1990年1月-2000年12月发生14例,占同期出生总数0.44％,其中有8例生前诊断为其他疾病,后经尸解病理证实。现将8例总结如下:临床资料一、一般资料男3例,女5例;发病年龄12h-3d4例、4-6d4例;出生体重≤1500g3例、1501-2500g2例、>2500g3例;早产4例(<32周2例、32-36周2例)、过期产1例、双胎2例;出生时轻度窒息3例、重度窒息2 Neonatal stomach wall muscle defects and perforation is a rare gastrointestinal disease. Our hospital from January 1990 to December 2000 occurred in 14 cases, accounting for the same period the total number of births 0.44%, of which 8 were diagnosed as other diseases before death, confirmed by autopsy pathology. 8 cases are summarized as follows: Clinical data First, the general information of 3 males and 5 females; onset age 12h-3d4 cases, 4-6d4 cases; birth weight ≤ 1500g3 cases, 1501-2500g2 cases,> 2500g3 cases; preterm4 (2 cases in 32 weeks and 2 cases in 32-36 weeks), 1 case of obstetric and 2 cases of twins, 3 cases of mild asphyxia at birth, severe asphyxia 2