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. Author manuscript; available in PMC: 2010 Jan 25.
Published in final edited form as: Prenat Diagn. 2005 Aug;25(8):683–686. doi: 10.1002/pd.1196

Table 1.

Review of the unbalanced karyotypes resulting from different segregation patterns in the carriers of t(11;22)

Karyotype Segregation Outcome Reference
47,XX/XY,+der(22)t(11;22)(q23;q11.2) 3 : 1 der(22) syndrome Zackai and Emanuel (1980); Shaikh et al. (1999)
47,XX,+der(22)t(11;22)(q23;q11.2) 2 : 2 adjacent-1(pat. de novo) + mat. MI
nondisjunction of chr 22
der(22) syndrome Dawson et al. (1996)
47,XX/XY,t(11;22)(q23;q11.2)pat, +der(22) ? 2 : 2 alternate + MII or postzygotic
nondisjunction of der(22)
der(22) syndrome Lockwood et al. (1989); Abeliovich and Carmi (1990); Lurie and Podelschuk (1992); Simi et al. (1992)
47,XX,t(11;22)(q23;q11.2)pat,+der(22) Crossover within chr 22 + 3 : 1 segregation der(22) syndrome Petkovic et al. (1996)
46,XX,der(22)t(11;22)(q23;q11.2)pat 2 : 2 adjacent-1 Empty sac (one of triplets) Soler et al. (1993)
46.XY,der(22)t(11;22)(q23;q11.2)mat/46,XY 2 : 2 or 3 : 1 with multiple postzygotic errors 26 year old with moderate mental retardation Kulharya et al. (2002)
45,XY,der(11)t(11;22)(q23;q11.2)mat,−22 3 : 1 Embryonic death at 7 weeks. This report