Tabardel Y, Soyeur D, Vivario E, Senterre J
Service de Pédiatrie, Université de Liège, CHU du Sart Tilman, Belgique.
Arch Fr Pediatr. 1989 Dec;46(10):737-40.
The authors report a case of infantile sialidosis with hydrops fetalis and heart failure. At birth the baby presented a dysmorphic syndrome with histological anomalies. A storage disease with deficiency of neuraminidase activity, sialidosis type II, was confirmed. Amniocentesis with sialic-acid dosage or thin-layed chromatography seems necessary in hydrops fetalis with heart failure of unknown origin.
作者报告了一例伴有胎儿水肿和心力衰竭的婴儿期涎酸沉积症病例。婴儿出生时表现出伴有组织学异常的畸形综合征。确诊为一种神经氨酸酶活性缺乏的贮积病,即II型涎酸沉积症。对于病因不明的伴有心力衰竭的胎儿水肿,进行唾液酸定量或薄层色谱法的羊膜穿刺术似乎是必要的。