Trisomy 22. Two new cases and delineation of the phenotype.

Two unrelated children, not affected with Down's syndrome, with strikingly similar phenotypes and an extra G-like chromosome are presented. Quinacrine and trypsin-Giemsa banding identified the extra chromosome as No. 22. The phenotype of these patients and the review of 15 additional similar cases from the literature permit a definition of the cardinal features of trisomy 22; mental and growth retardation, microcephaly and craniofacial asymmetry, strabismus, beaked and prominent nose, long philtrum, cleft palate, micrognathia, large low set ears with preauricular tags and/or pits, long slender fingers, congenital heart disease, inguinal hernia, and hip dislocation.

[1]  B. Crandall,et al.  Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding. , 1973, Annales de genetique.

[2]  J. Scheres Human chromosome banding. , 1972, Lancet.

[3]  K. Gustavson,et al.  Three non‐mongoloid patients of similar phenotype with an extra G‐like chromosome , 1972, Clinical genetics.

[4]  K. Hirschhorn,et al.  Trisomy 22: a clinical entity. , 1971, The Journal of pediatrics.

[5]  N. Sadan,et al.  The question of trisomy 22 syndrome. , 1971, The Journal of pediatrics.

[6]  T. Caspersson,et al.  Differential binding of alkylating fluorochromes in human chromosomes. , 1970, Experimental cell research.

[7]  M. Mikkelsen,et al.  Additional small acrocentric chromosome: two cases. , 2008, Journal of mental deficiency research.

[8]  I. Uchida,et al.  Familial occurrence of trisomy 22. , 1968, American journal of human genetics.

[9]  G. J. Cunningham,et al.  VENTILATION OF OPERATING-THEATRES. , 1964, Lancet.

[10]  B. Hall Mongolism and Other Abnormalities in a Family with Trisomy 21–22 Tendency , 1963, Acta paediatrica. Supplementum.

[11]  H. Zellweger,et al.  Two cases of multiple malformations with an autosomal chromosomal aberration- partial trisomy D? , 1962, Helvetica paediatrica acta.