TRISOMY-22 AND INTERSEX

Authors
NICHOLL RM GRIMSLEY L BUTLER L PALMER RW REES HC SAVAGE MO COSTELOE K
Citation
Rm. Nicholl et al., TRISOMY-22 AND INTERSEX, Archives of Disease in Childhood, 71(1), 1994, pp. 60000057-60000058
Citations number
6
Categorie Soggetti
Pediatrics
Journal title
Archives of Disease in Childhood → ACNP
ISSN journal
00039888
Volume
71
Issue
1
Year of publication
1994
Pages
60000057 - 60000058
Database
ISI
SICI code
0003-9888(1994)71:1<60000057:TAI>2.0.ZU;2-S
Abstract
Complete trisomy 22, with or without mosaicism, has been reported as a distinct syndrome. In this report an infant is described who was exte rnally male but with female rudimentary internal organs and whose kary otype was 47, XX+22.