Tanphaichitr V S, Suvatte V, Tuchinda S, Mahasandana C, Wenger D A
Southeast Asian J Trop Med Public Health. 1979 Dec;10(4):562-7.
The first case of Niemann-Pick disease Type A in a Thai infant was reported. The patient also had abnormal hemoglobin E. The diagnosis was based on the clinical features, bone marrow findings and sphingomyelinase levels in the culture of skin fibroblasts. The autosomal recessive mode of inheritance was confirmed in this case.
泰国一名婴儿被报告为第一例A型尼曼-匹克病患者。该患者还患有异常血红蛋白E。诊断基于临床特征、骨髓检查结果以及皮肤成纤维细胞培养中的鞘磷脂酶水平。此病例证实为常染色体隐性遗传模式。