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Congenital microcephaly: phenotypic features in a consecutive sample of newborn infants
J E Vargas1, E N Allred, A Leviton
1Division of Genetics and the Neuroepidemiology Unit, Children's Hospital, Boston, USA.
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.