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Apparently nonmosaic trisomy 22: clinical report and review
T S Sundareshan1, K K Naguib, S A al-Awadi
1Kuwait Medical Genetics Centre, Maternity Hospital, Safat.
American Journal of Medical Genetics
|May 1, 1990
Abstract:
We report on apparently nonmosaic trisomy 22 in a liveborn girl with multiple congenital anomalies. The abnormalities were growth retardation; microcephaly; hypertelorism; epicanthic folds; anti-mongoloid slant; apparently low-set, malformed ears; highly arched, cleft palate; short webbed neck; and hypoplastic nails. The extra 22 was found to be of maternal origin by chromosome polymorphism.