A case of trisomy 22 with a probable Robertsonian translocation 21/22
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 45 (2) , 219-223
- https://doi.org/10.1007/bf00286967
Abstract
A 2-year-old girl with a probable trisomy-22 translocation is described. The principal clinical symptoms described by the authors who have reported cases with proved trisomy 22 are presented. A probable 46, XX,-21,+t(21q;22q) karyotype was established in the patient. The proband's clinical picture is compared with other trisomy 22 cases described in the literature. The incidence of this trisomy among the human population is discussed.This publication has 17 references indexed in Scilit:
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