11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features.

摘要

The clinical findings in patients with 11q deletion, range from an apparently normal phenotype [Li et al, 2002; Goumy et al., 2008] in the absence of mental retardation [Sorensen et al., 1979; Rudd and Teshima, 1983; Ikegawa et al., 1998; Bateman et al., 1984; Sparkes et al., 2009] to dysmorphic features with developmental delay [McPherson and Meissner, 1982; Taki et al., 1983; Okamura et al., 1988; Stratton et al., 1994; Ono et al., 1996; Li et al., 2006].