Cavallotti G P, Genovese M G, Bocchini R
Minerva Pediatr. 1989 May;41(5):273-6.
A rare case of sirenomelia malformation in a fetus of 33 weeks is reported. Besides typical fusion of the lower extremities, important alterations of the urogenital system and large intestine are present. A review of the literature on the subject is presented. The usefulness of ultrasonography in the prenatal diagnosis of this malformation is then stressed.
报道了一例33周胎儿的罕见并腿畸形病例。除了典型的下肢融合外，泌尿生殖系统和大肠也有重要改变。本文对该主题的文献进行了综述。随后强调了超声检查在这种畸形产前诊断中的作用。
