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. 1994 Jul;71(1):F57-8.
doi: 10.1136/fn.71.1.f57.

Trisomy 22 and intersex

R M Nicholl  1 , L Grimsley, L Butler, R W Palmer, H C Rees, M O Savage, K Costeloe
Affiliations

Trisomy 22 and intersex

R M Nicholl et al. Arch Dis Child Fetal Neonatal Ed. 1994 Jul.

Abstract

Complete trisomy 22, with or without mosaicism, has been reported as a distinct syndrome. In this report an infant is described who was externally male but with female rudimentary internal organs and whose karyotype was 47,XX+22.

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