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Case Reports
. 1976 Dec;13(6):517-20.
doi: 10.1136/jmg.13.6.517.

Confirmation of trisomy 22 by trypsin-giemsa staining

M L Begleiter, P Kulkarni, D J Harris
Case Reports

Confirmation of trisomy 22 by trypsin-giemsa staining

M L Begleiter et al. J Med Genet. 1976 Dec.

Abstract

A small-for-dates male infant with mental retardation, microcephaly, malformed ears, preauricular sinuses, epicanthal folds, micrognathia, congenital heart diseases, micropenis, and micropolygyria of the parietal and occipital lobes of the cerebral cortex was shown to have a 47,XY,+22 karyotype by trypsin-giemsa banding. Review of reported cases confirms that there may be distinctive trisomy 22 syndrome.

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References

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