Congenital microcephaly: Phenotypic features in a consecutive sample of newborn infants

被引:23
作者
Vargas, JE
Allred, EN
Leviton, A
Holmes, LB
机构
[1] Massachusetts Gen Hosp, Serv Pediat, Genet & Teratol Unit, Boston, MA 02114 USA
[2] Childrens Hosp, Div Genet, Boston, MA 02115 USA
[3] Childrens Hosp, Neuroepidemiol Unit, Boston, MA 02115 USA
关键词
D O I
10.1067/mpd.2001.115314
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: We compared the prevalence of major and minor anomalies in a consecutive sample of newborn infants with congenital microcephaly with that among normocephalic infants. Study design: Head measurements from >19,000 liveborn infants at 1 hospital during the years 1991 and 1992 were reviewed. Infants whose head circumference was in the lowest quartile (n = 850) were remeasured by research assistants to identify all whose head circumference was 2 SD below the mean for gestational age; 106 infants with congenital microcephaly were identified. Infants with microcephaly (n = 65) and 294 infants in a control group were examined systematically for major malformations and minor physical features. Results: Four (6.2%) of the 65 infants examined either had a major malformation or were considered dysmorphic. One of the 4 had a specific multiple malformation syndrome, and 1 dysmorphic infant had a rare metabolic defect. Overall, the infants with microcephaly did not have a higher frequency of minor anomalies. However, there was a higher frequency of frontal bossing, small chin, and short nose with anteverted nares, which was associated with small body size rather than microcephaly. Conclusions: Congenital microcephaly is infrequently accompanied by major malformations and occurs rarely as part of a recognizable syndrome.
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页码:210 / 214
页数:5
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