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A case of monosomy 21
B Garzicić1, M Guć-Sćekić, G Pilić-Radivojević
1Institut za zdravstvenu zastitu majke i deteta Srbije, Laboratorija za citogenetiku, Novi Beograd, Yugosiavia.
Annales De Genetique
|January 1, 1988
Abstract:
A new case of monosomy 21 was observed in a newborn male. Characteristic clinical features include: an antimongoloid eye slants, large and low set ears, flat nose bridge, hypoplastic nipples, cardiac anomalies, muscular hypotonia, retarded psychomotor development. The karyotypes of the parents were normal.