Guc-Scekic M, Milasin J, Stevanovic M, Stojanov L J, Djordjevic M
Laboratory of Medical Genetics, Mother and Child Health Institute, Dr Vukan Cupic, Belgrade, Yugoslavia.
Clin Genet. 2002 Jan;61(1):62-5. doi: 10.1034/j.1399-0004.2002.610112.x.
Liveborn infants with tetraploidy are very rare in human pregnancies and usually die during the first days or months. Seven cases of liveborn infants with tetraploidy have previously been reported. Among them only two 92, XXXX infants survived for longer than 12 months. Here we report on the case of a 26-month-old girl with tetraploidy. The main clinical features of tetraploidy are facial dysmorphism, severely delayed growth and developmental delay. On the basis of molecular studies we discuss the possible origin of the additional chromosome sets in our proband. To our knowledge, this infant is the first reported case of tetraploidy who lived up to 26 months.
在人类妊娠中,活产的四倍体婴儿非常罕见,通常在出生后的头几天或几个月内死亡。此前曾报道过7例活产四倍体婴儿。其中只有两名92,XXXX婴儿存活超过12个月。在此,我们报告一例26个月大的四倍体女孩病例。四倍体的主要临床特征为面部畸形、严重生长发育迟缓。基于分子研究,我们讨论了先证者中额外染色体组的可能来源。据我们所知,这名婴儿是首例报道的存活至26个月的四倍体病例。