Bromley B, Benacerraf B R
Department of Obstetrics and Gynecology, Massachusetts General Hospital, Brigham & Women's Hospital, Harvard Medical School, Boston, USA.
J Ultrasound Med. 1995 Apr;14(4):303-6. doi: 10.7863/jum.1995.14.4.303.
Our objective was to determine whether the diagnosis of microcephaly present at birth is apparent using standard biometry in the second trimester. Fetuses with prenatally suspected microcephaly (biparietal diameter > or = 3 standard deviations below mean) who had a first sonogram prior to 22 weeks' gestation and a confirmation of microcephaly after birth were included in the study. We excluded all fetuses who had neural tube defects or other major associated abnormality that would lead to a suspicion of microcephaly. We therefore included fetuses who either had normal-appearing brains sonographically or intracranial calcifications as the only sonographic abnormality seen prior to 22 weeks' gestation. Seven fetuses met these criteria. One fetus was diagnosed as having microcephaly prior to 22 weeks' gestation. The other six fetuses had a normal head size prior to 22 weeks' gestation and were diagnosed as having microcephaly at 27 weeks' gestation and later. Only one of the seven fetuses had a karyotypic abnormality. We conclude that the prenatal diagnosis of microcephaly is not excluded by normal biometry on second trimester sonography.
我们的目的是确定在孕中期使用标准生物测量法能否明确诊断出生时即存在的小头畸形。本研究纳入了妊娠22周前首次超声检查时产前怀疑小头畸形(双顶径大于或等于低于均值3个标准差)且出生后确诊为小头畸形的胎儿。我们排除了所有患有神经管缺陷或其他主要相关异常(这些异常会导致怀疑小头畸形)的胎儿。因此,我们纳入了超声检查时大脑外观正常或在妊娠22周前仅发现颅内钙化作为唯一超声异常的胎儿。7例胎儿符合这些标准。1例胎儿在妊娠22周前被诊断为小头畸形。其他6例胎儿在妊娠22周前头围正常,在妊娠27周及以后被诊断为小头畸形。7例胎儿中只有1例有染色体核型异常。我们得出结论,孕中期超声检查时正常生物测量法不能排除小头畸形的产前诊断。